Thermodynamic and composition information

The subset of oligonucleotide sequences shown here was created by Dr. Kretschmer-Kazemi Far. The oligonucleotides that target known polymorphic sites of mRNAs,introns or the oligonucleotides that represent mismatched variants with their mRNAs target were removed from the set that was described previously (Bioinformatics 2000 Sep;16(9):843-844). Thermodynamic values for this table were calculated by program OligoWalk from RNAstructure 7 package (http://128.151.176.70/RNAstructure.html). For any questions related to this dataset, please contact Olga Matveeva.

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															Assay Type		double or not
Oligo sequence	Antisense efficiency	Oligo-RNA	Target	Oligo-	Oligo-Oligo	%A	%G	%C	%T	Reference	Target name	accession	Target position	Concentration	(R=RNA, P=Protein)	Length	in the datbse
		duplex formation	RNA structure	intramolecular structure	intermolecular structure							number
		kcal/mol	kcal/mol	kcal/mol	kcal/mol									nM
TGACAGTTGGTTTCTTTTCC	0.85	-23.4	-9.5	0	-3.7	10	20	20	50	S.P. Ho et. al, 1996	MDR	M14758	508	1000	P	20
ACTGACAGTTGGTTTCTTTT	0.84	-22.1	-9.5	0	-4.4	15	20	15	50	S.P. Ho et. al, 1996	MDR		510	1000	P	20
ACACTGACAGTTGGTTTCTT	0.65	-22.8	-9.5	0	-4.8	20	20	20	40	S.P. Ho et. al, 1996	MDR		512	1000	P	20
TTTATTGTTCAGTTTAAAAA	0.92	-14.7	-7.6	0	-4.8	35	10	5	50	S.P. Ho et. al, 1996	MDR		471	1000	P	20
ACTTTTATTGTTCAGTTTAA	0.97	-18	-4.6	0	-2.3	25	10	10	55	S.P. Ho et. al, 1996	MDR		474	1000	P	20
TCTTCTTTGCTCCTCCATTG	0.67	-26.1	-8.5	0	-3.6	5	10	35	50	S.P. Ho et. al, 1996	MDR		445	1000	P	20
TCTTCTTCTTTGCTCCTCCA	0.7	-27.4	-6.7	0	-3.6	5	5	40	50	S.P. Ho et. al, 1996	MDR		448	1000	P	20
AGTTCTTCTTCTTTGCTCCT	0.92	-25.6	-10.5	0	-3.6	5	10	30	55	S.P. Ho et. al, 1996	MDR		451	1000	P	20
TCCATTGCGGTCCCCTTCAA	0.2	-30	-9.6	0	-4	15	15	40	30	S.P. Ho et. al, 1996	MDR		432	1000	P	20
TCCTCCATTGCGGTCCCCTT	0	-32.9	-4.2	0	-4	5	15	45	35	S.P. Ho et. al, 1996	MDR		435	1000	P	20
TGCTCCTCCATTGCGGTCCC	0.09	-32.6	-12.1	-0.6	-4	5	20	45	30	S.P. Ho et. al, 1996	MDR		438	1000	P	20
GACCTCGCGCTCCTTGGAAC	0.17	-28.9	-11.4	0	-7	15	25	40	20	S.P. Ho et. al, 1996	MDR		402	1000	P	20
CCGACCTCGCGCTCCTTGGA	0.15	-32.2	-11.4	0	-7.1	10	25	45	20	S.P. Ho et. al, 1996	MDR		404	1000	P	20
ATCCCGACCTCGCGCTCCTT	0	-32.8	-11.4	0	-7.5	10	15	50	25	S.P. Ho et. al, 1996	MDR		407	1000	P	20
GCTCCTTGGAACGGCCACCA	0.18	-30.8	-14.5	-1.1	-7.9	20	25	40	15	S.P. Ho et. al, 1996	MDR		394	1000	P	20
GCGCTCCTTGGAACGGCCAC	0.15	-30.7	-12.6	-1.1	-9.2	15	30	40	15	S.P. Ho et. al, 1996	MDR		396	1000	P	20
TCCGACTTTAGTGGAAAGAC	0.9	-21.2	-18.5	-0.9	-6.7	30	25	20	25	S.P. Ho et. al, 1996	MDR		348	1000	P	20
TACTCCGACTTTAGTGGAAA	0.84	-21.2	-12.8	-1.1	-6.6	30	20	20	30	S.P. Ho et. al, 1996	MDR		351	1000	P	20
AGCTTGGAAGAGCCGCTACT	0.54	-26.6	-28.9	-2.5	-7.6	25	30	25	20	S.P. Ho et. al, 1996	MDR		294	1000	P	20
TGAGCTTGGAAGAGCCGCTA	0.54	-26.1	-24.8	-2.5	-8.4	25	35	20	20	S.P. Ho et. al, 1996	MDR		296	1000	P	20
GCCTGGGAGGGTATTCAGCT	0.58	-28.9	-31.1	-0.8	-5.8	15	40	20	25	C.F. Bennett et. al, 1994	VCAM-1	NM_001078 (Variante 1; 3119 bp)	35	50	P	20
CCTGTGTGTGCCTGGGAGGG	0.88	-30.6	-19.6	-0.8	-4.9	5	50	20	25	C.F. Bennett et. al, 1994	VCAM-1		44	50	P	20
GGCATTTTAAGTTGCTGTCG	0.34	-23.4	-8.6	-1.5	-6.5	15	30	15	40	C.F. Bennett et. al, 1994	VCAM-1		106	50	P	20
CAGCCTGCCTTACTGTGGGC	0.67	-30.4	-12.9	-1.7	-7.9	10	30	35	25	C.F. Bennett et. al, 1994	VCAM-1		741	50	P	20
CTTGAACAATTAATTCCACCT	0.37	-21.4	-4.4	0	-6	33.3	4.8	28.6	33.3	C.F. Bennett et. al, 1994	VCAM-1		1028	50	P	21
CTGTGTCTCCTGTCTCCGCT	0.27	-30.3	-16.2	0	-3.1	0	20	40	40	C.F. Bennett et. al, 1994	VCAM-1		2034	50	P	20
GTCTTTGTTGTTTTCTCTTCC	0.42	-25.5	-10.4	0	-0.3	0	14.3	23.8	61.9	C.F. Bennett et. al, 1994	VCAM-1		2179	50	P	21
TGAACATATCAAGCATTAGC	0.53	-19	-6.6	-0.9	-5.3	40	15	20	25	C.F. Bennett et. al, 1994	VCAM-1		2340	50	P	20
GCAATCTTGCTATGGCATAA	0.48	-22.3	-25.6	-1.7	-8	30	20	20	30	C.F. Bennett et. al, 1994	VCAM-1		2616	50	P	20
CCCGGCATCTTTACAAAACC	0.5	-24.7	-25.3	0	-6.1	30	10	40	20	C.F. Bennett et. al, 1994	VCAM-1		2822	50	P	20
AACCCAGTGCTCCCTTTGCT	0.21	-30.3	-17.4	-0.4	-3.6	15	15	40	30	C.F. Bennett et. al, 1994	VCAM-1		2868	50	P	20
AACATCTCCGTACCATGCCA	0.25	-27	-21.3	0	-4.2	30	10	40	20	C.F. Bennett et. al, 1994	VCAM-1		2953	50	P	20
GGCCACATTGGGAAAGTTGC	0.29	-25.4	-21	-1	-7	25	35	20	20	C.F. Bennett et. al, 1994	VCAM-1		3001	50	P	20
CCGTGCTCATGGTGTCCTTTC	0.51	-30.2	-15.4	0	-5.3	4.8	23.8	33.3	38.1	G.C. Tu et. al, 1998	TNF	L00981woInt	152	1000	P	21
GATCATGCTTTCCGTGCTCAT	0.94	-27.7	-20	-0.4	-5.1	14.3	19	28.6	38.1	G.C. Tu et. al, 1998	TNF		163	1000	P	21
TAGACGATAAAGGGGTCAGAG	1	-21.6	-4.1	-1.2	-4.6	38.1	38.1	9.5	14.3	G.C. Tu et. al, 1998	TNF		932	1000	P	21
AGTGAGTTCCGAAAGCCCATT	0.94	-27	-24.1	0	-3.4	28.6	23.8	23.8	23.8	G.C. Tu et. al, 1998	TNF		1123	1000	P	21
TGATCCACTCCCCCCTCCACT	0.06	-35.2	-29.5	0	-4.3	14.3	4.8	57.1	23.8	G.C. Tu et. al, 1998	TNF		1180	1000	P	21	double
AGGGAAGGAAGGAAGGAAGGG	1	-22.9	-28.1	0	0	42.9	57.1	0	0	G.C. Tu et. al, 1998	TNF		1244	1000	P	21
CAGTCTGGGAAGCTCTGAGGG	1	-27.4	-34.3	-1.2	-7.8	19	42.9	19	19	G.C. Tu et. al, 1998	TNF		1265	1000	P	21
GGTTCCGTAAGGAAGGCTGG	0.94	-26.1	-22.2	-3.9	-12.4	20	45	15	20	G.C. Tu et. al, 1998	TNF		1304	1000	P	20
AATAATAAATAATAAATAAAT	1	-7.1	-3.2	0	-1.2	71.4	0	0	28.6	G.C. Tu et. al, 1998	TNF		1352	1000	P	21
TTCCCAACGCTGGGTCCTCCA	1	-33.1	-25.1	-2.9	-8.6	14.3	19	42.9	23.8	G.C. Tu et. al, 1998	TNF		1419	1000	P	21
GGGATAGCTGGTAGTTTAG	1	-21.7	-4.4	0	-4.5	21.1	42.1	5.3	31.6	G.C. Tu et. al, 1998	TNF		1478	1000	P	19
CTGGTCCCTTGGTGTCCTCGC	0.69	-33.5	-32.6	0	-3.3	0	28.6	38.1	33.3	G.C. Tu et. al, 1998	TNF		12	1000	P	21
TTGCTGTTCTCCCTCCTGGCT	0.15	-32.8	-23	0	-4.3	0	19	38.1	42.9	G.C. Tu et. al, 1998	TNF		31	1000	P	21
GCAGCCTTGTCCCTTGAAGAG	0.73	-29.3	-16	0	-3.5	19	28.6	28.6	23.8	G.C. Tu et. al, 1998	TNF		586	1000	P	21
CTTGAGCTCAGCTCCCTCAGG	0.45	-30.6	-18.4	-2.5	-11.5	14.3	23.8	38.1	23.8	G.C. Tu et. al, 1998	TNF		712	1000	P	21
GCTGGAAGACTCCTCCCAGGT	0.35	-31.2	-33.9	-2	-7.6	19	28.6	33.3	19	G.C. Tu et. al, 1998	TNF		752	1000	P	21
GCTGAGCAGGTCCCCCTTCTC	0.8	-34.2	-16.7	-0.8	-5.6	9.5	23.8	42.9	23.8	G.C. Tu et. al, 1998	TNF		775	1000	P	21
TCCACTCCCCCGATCCACTCA	0.11	-34.2	-35	0	-3.9	19	4.8	57.1	19	G.C. Tu et. al, 1998	TNF		1165	1000	P	21	double
TGATCCACTCCCCCCTCCACT	0.1	-35.2	-29.5	0	-4.3	14.3	4.8	57.1	23.8	G.C. Tu et. al, 1998	TNF		1180	1000	P	21	double
GCCTGAAGACAGCTTCCCAAC	0.24	-28.4	-30.6	-2.1	-6.3	28.6	19	38.1	14.3	G.C. Tu et. al, 1998	TNF		1432	1000	P	21
CAGTCACGGCTCCCGTGGG	0.91	-29.8	-20.9	-4.5	-11.9	10.5	36.8	36.8	15.8	G.C. Tu et. al, 1998	TNF		1636	1000	P	19
CCCCCGATCCACTCAGGCATC	0.82	-33.7	-28.9	0.1	-4	19	14.3	52.4	14.3	G.C. Tu et. al, 1998	TNF		1159	1000	P	21
ACTCCCCCGATCCACTCAGGC	0.1	-34.1	-30.8	-0.1	-3.9	19	14.3	52.4	14.3	G.C. Tu et. al, 1998	TNF		1162	1000	P	21
TCCACTCCCCCGATCCACTCA	0.08	-34.2	-35	0	-3.9	19	4.8	57.1	19	G.C. Tu et. al, 1998	TNF		1165	1000	P	21	double
CCCTCCACTCCCCCGATCCAC	0.11	-37.1	-35.3	0	-3.9	14.3	4.8	66.7	14.3	G.C. Tu et. al, 1998	TNF		1168	1000	P	21
CCCCCCTCCACTCCCCCGATC	0.08	-40.2	-34.8	0	-3.5	9.5	4.8	71.4	14.3	G.C. Tu et. al, 1998	TNF		1171	1000	P	21
ACTCCCCCCTCCACTCCCCCG	0.09	-40.7	-33.8	0	-2.2	9.5	4.8	71.4	14.3	G.C. Tu et. al, 1998	TNF		1174	1000	P	21
TCCACTCCCCCCTCCACTCCC	0.08	-39	-37.6	0	0	9.5	0	71.4	19	G.C. Tu et. al, 1998	TNF		1177	1000	P	21
GCCTGATCCACTCCCCCCTCC	0.12	-38.1	-34.6	0	-4.3	9.5	9.5	61.9	19	G.C. Tu et. al, 1998	TNF		1183	1000	P	21
TCCACTCCCCCGATCCACTCA	0.1	-34.2	-35	0	-3.9	19	4.8	57.1	19	G.C. Tu et. al, 1998	TNF		1165	1000	P	21	double
TGATCCACTCCCCCCTCCACT	0.08	-35.2	-29.5	0	-4.3	14.3	4.8	57.1	23.8	G.C. Tu et. al, 1998	TNF		1180	1000	P	21	double
CGGGGCCGCAACGCCGCCTG	0.95	-35.1	-33.9	-3	-9.3	10	40	45	5	A.J. Stewart et. al, 1996	MRP	NM_004996	2	500	P	20
GGTGATCGGGCCCGGTTGCT	0.68	-32.4	-20.9	-0.3	-14.8	5	45	25	25	A.J. Stewart et. al, 1996	MRP		141	500	P	20
CCGGTGGCGCGGGCGGCGGC	0.69	-37.4	-10.4	-2.9	-11.4	0	60	35	5	A.J. Stewart et. al, 1996	MRP		176	500	P	20
AGCCCCGGAGCGCCATGCCG	0.74	-36.1	-28.2	-0.9	-8.3	15	35	45	5	A.J. Stewart et. al, 1996	MRP		193	500	P	20
TCGGAGCCATCGGCGCTGCA	0.8	-31.7	-16.4	-1.7	-8.7	15	35	35	15	A.J. Stewart et. al, 1996	MRP		215	500	P	20
GGCACCCACACGAGGACCGT	0.79	-31.1	-27.9	-1	-6	25	30	40	5	A.J. Stewart et. al, 1996	MRP		302	500	P	20
TGCTGTTCGTGCCCCCGCCG	0.51	-35.6	-15	-1	-5.6	0	30	45	25	A.J. Stewart et. al, 1996	MRP		2107	500	P	20
CGCGCTGCTTCTGGCCCCCA	0.56	-35.9	-26.7	-0.7	-8.8	5	25	50	20	A.J. Stewart et. al, 1996	MRP		2503	500	P	20
GCGGCGATGGGCGTGGCCAG	0.73	-32.9	-10.6	-2.8	-11.4	10	55	25	10	A.J. Stewart et. al, 1996	MRP		3524	500	P	20
CAGGAGGTCCGATGGGGCGC	0.95	-30.7	-18.7	-1.7	-9.2	15	50	25	10	A.J. Stewart et. al, 1996	MRP		4722	500	P	20
GCTCACACCAAGCCGGCGTC	0.78	-30.9	-19.3	-0.2	-12.1	20	25	45	10	A.J. Stewart et. al, 1996	MRP		4775	500	P	20
AGGCCCTGCAGTTCTGACCA	0.95	-30.5	-7.4	-0.7	-7.7	20	25	35	20	A.J. Stewart et. al, 1996	MRP		4812	500	P	20
CTCCTCCCTGGGCGCTGGCA	0.74	-34.9	-37.8	-1.6	-8.2	5	30	45	20	A.J. Stewart et. al, 1996	MRP		4835	500	P	20
ACCGGATGGCGGTGGCTGCT	0.73	-31.6	-20.1	-3.1	-13.8	10	45	25	20	A.J. Stewart et. al, 1996	MRP		4938	500	P	20
CGCATCTCTGTCTCTCCTGG	0.77	-28.2	-21.6	0	-4	5	20	40	35	A.J. Stewart et. al, 1996	MRP		4985	500	P	20
GGGTTGAAGCCATTGCAGGG	0.45	-27.1	-17.2	-1.4	-6.6	20	45	15	20	S.M. Stepkowski et. al, 1994	ICAM-1	M31585	52	300	P	20
CTCATCCAGCAGGCTCAGGG	0.75	-29	-24.4	0.4	-4.9	20	30	35	15	S.M. Stepkowski et. al, 1994	ICAM-1		1667	300	P	20
CCAGAGGAAGTGGCTGAGGG	0.35	-26.5	-29.3	-0.2	-4.4	25	50	15	10	S.M. Stepkowski et. al, 1994	ICAM-1		1756	300	P	20
TGCATCCCCCAGGCCACCAT	0	-34.2	-28.7	-0.3	-7.7	20	15	50	15	S.M. Stepkowski et. al, 1994	ICAM-1		1791	300	P	20
CAAGTGTGCATCCCCCAGGC	0	-31	-16.7	0	-8.7	20	25	40	15	S.M. Stepkowski et. al, 1994	ICAM-1		1797	300	P	20
TTGGGACAATGTCTCAGCTT	0.25	-23.7	-13.8	-1.5	-10.6	20	25	20	35	S.M. Stepkowski et. al, 1994	ICAM-1		2020	300	P	20
TGCCAGTCCACATAGTGTTT	0.25	-26	-20.3	-0.3	-4.4	20	20	25	35	S.M. Stepkowski et. al, 1994	ICAM-1		2255	300	P	20
TGCTTACCCTCCCACAGCAG	0.1	-30.1	-28.6	-1.1	-4.8	20	15	45	20	S.M. Stepkowski et. al, 1994	ICAM-1		2471	300	R	20
CGGGAGGCGGTCACATTCGG	0.25	-28.5	-18.5	-0.1	-4	15	45	25	15	B.P. Monia et. al, 1996	c-raf	XM_051583	1	200	R	20
GGTGAGGGAGCGGGAGGCGG	0.98	-30.6	-30.3	-1.5	-4.1	15	70	10	5	B.P. Monia et. al, 1996	c-raf		11	200	R	20
TCCTCCTCCCCGCGGCGGGT	0.95	-37.8	-18.8	-3.2	-16.7	0	30	50	20	B.P. Monia et. al, 1996	c-raf		28	200	R	20
CGCTCCTCCTCCCCGCGGCG	0.35	-37.7	-26.9	-0.9	-10.5	0	25	60	15	B.P. Monia et. al, 1996	c-raf		31	200	R	20
CTCGCCCGCTCCTCCTCCCC	1	-38.4	-39.1	0	-3.2	0	10	70	20	B.P. Monia et. al, 1996	c-raf		37	200	R	20
TTCTCGCCCGCTCCTCCTCC	0.65	-34.9	-35.9	0	-3.1	0	10	60	30	B.P. Monia et. al, 1996	c-raf		39	200	R	20
TTCGGCGGCAGCTTCTCGCC	0.37	-31.9	-29	-3.2	-12	5	30	40	25	B.P. Monia et. al, 1996	c-raf		51	200	R	20
GCCGCCCCAACGTCCTGTCG	0.42	-34.3	-16	0	-5.2	10	25	50	15	B.P. Monia et. al, 1996	c-raf		71	200	R	20
ATTCTTAAACCTGAGGGAGC	1	-22.3	-12.4	-0.6	-4.5	30	25	20	25	B.P. Monia et. al, 1996	c-raf		94	200	R	20
GATGCAGCTTAAACAATTCT	0.99	-19.8	-4.1	0	-4.9	35	15	20	30	B.P. Monia et. al, 1996	c-raf		109	200	R	20
CCCTGTATGTGCTCCATTGA	0.38	-27.5	-8.9	0	-3.9	15	20	30	35	B.P. Monia et. al, 1996	c-raf		127	200	R	20
GGTGCAAAGTCAACTAGAAG	0.88	-19.8	-10.9	0	-5.4	40	30	15	15	B.P. Monia et. al, 1996	c-raf		2070	200	R	20
TTCTCCTCCTCCCCTGGCAG	0.8	-33	-21.5	0	-4.1	5	15	50	30	B.P. Monia et. al, 1996	c-raf		2100	200	R	20
CTGGCTTCTCCTCCTCCCCT	0.95	-34.1	-22.5	-0.5	-3.7	0	10	55	35	B.P. Monia et. al, 1996	c-raf		2105	200	R	20
CCTGCTGGCTTCTCCTCCTC	0.92	-31.9	-18.4	-0.5	-5.9	0	15	50	35	B.P. Monia et. al, 1996	c-raf		2109	200	R	20
CAGCACTGCAAATGGCTTCC	0.8	-25.8	-22	-1.1	-6.6	25	20	35	20	B.P. Monia et. al, 1996	c-raf		2265	200	R	20
TTGAGCATGGGGAATGTGGG	0.63	-24.3	-11	-0.4	-4.3	20	50	5	25	B.P. Monia et. al, 1996	c-raf		2302	200	R	20
ACCATCAACATCCACTTGCG	1	-25.1	-9.4	0	-4	30	10	40	20	B.P. Monia et. al, 1996	c-raf		2342	200	R	20
TGTAGCCAACAGCTGGGGCT	0.96	-28.6	-18.8	-2.2	-15.6	20	35	25	20	B.P. Monia et. al, 1996	c-raf		2382	200	R	20
TCAGGGCTGGACTGCCTGCT	0.52	-30.5	-24.1	-2.4	-9.4	10	35	30	25	B.P. Monia et. al, 1996	c-raf		2425	200	R	20
CTGATTTCCAAAATCCCATG	0.26	-21.8	-18.7	-1.9	-7.3	30	10	30	30	B.P. Monia et. al, 1996	c-raf		2455	200	R	20
TCCCGCCTGTGACATGCATT	0.05	-29.2	-6.7	-0.5	-6.7	15	20	35	30	B.P. Monia et. al, 1996	c-raf		2485	200	R	20
TCTGGCGCTGCACCACTCTC	0.25	-30	-23.3	-0.7	-8.1	10	20	45	25	B.P. Monia et. al, 1996	c-raf		2514	200	R	20
GTCTGGCGCTGCACCACTCT	0.35	-30.8	-22	-0.5	-7.3	10	25	40	25	B.P. Monia et. al, 1996	c-raf		2515	200	R	20
CTGGGCTGTTTGGTGCCTTA	0.8	-28.3	-23.3	-2.3	-7.8	5	35	20	40	B.P. Monia et. al, 1996	c-raf		2545	200	R	20
GCCGAGTGCCTTGCCTGGAA	0.98	-31	-11.9	-0.5	-5	15	35	30	20	B.P. Monia et. al, 1996	c-raf		2678	200	R	20
CTGAGAGGGCTGAGATGCGG	1	-26.2	-8.1	-0.8	-4.3	20	50	15	15	B.P. Monia et. al, 1996	c-raf		2702	200	R	20
GCTCCTGGAAGACAAAATTC	0.82	-21	-24.7	0	-6.1	35	20	25	20	B.P. Monia et. al, 1996	c-raf		2743	200	R	20
TGTGACTAGAGAAACAAGGC	0.68	-19.6	-20.7	0	-3.6	40	30	15	15	B.P. Monia et. al, 1996	c-raf		2825	200	R	20
CAAGAAAACCTGTATTCCTG	1	-19.9	-12.1	0	-3.3	35	15	25	25	B.P. Monia et. al, 1996	c-raf		2865	200	R	20
TTGTCAGGTGCAATAAAAAC	0.88	-17.7	-9.8	0	-5.4	40	20	15	25	B.P. Monia et. al, 1996	c-raf		2905	200	R	20
TTAAAATAACATAATTGAGG	0.93	-12.5	-9.8	0	-2.9	50	15	5	30	B.P. Monia et. al, 1996	c-raf		2945	200	P	20
GCGTCGACTGGGGCGCGTGAT	0.95	-32.2	-19.6	-2.7	-8.8	9.5	47.6	23.8	19	C.H. Lee et. al, 1995	ICAM-1	M31585	10	100	P	21
GAGGAGCTCAGCGTCGACTG	0.83	-26.9	-22.6	-0.4	-9.2	20	40	25	15	C.H. Lee et. al, 1995	ICAM-1		21	100	P	20	double
GGAGCTCAGCGTCGA	0.85	-20.7	-20.6	-0.7	-9.2	20	40	26.7	13.3	C.H. Lee et. al, 1995	ICAM-1		24	100	P	15
TCTGAGTAGCAGAGGAGCTCAG	0.33	-27.3	-18.2	-2.8	-13.5	27.3	36.4	18.2	18.2	C.H. Lee et. al, 1995	ICAM-1		30	100	P	22
TCTGAGTAGCAGAGGAGCTCA	0.3	-26.4	-15.5	-1.6	-13.5	28.6	33.3	19	19	C.H. Lee et. al, 1995	ICAM-1		31	100	P	21
CTCTGAGTAGCAGAGGAGCTC	0.17	-26.6	-13.8	-3.1	-15.4	23.8	33.3	23.8	19	C.H. Lee et. al, 1995	ICAM-1		32	100	P	21
GAGTAGCAGAGGAGC	0.61	-17.7	-9.1	0	-3.9	33.3	46.7	13.3	6.7	C.H. Lee et. al, 1995	ICAM-1		34	100	P	15
CTCTGAGTAGCAGAGG	0.76	-18.4	-8.7	-3.1	-8.2	25	37.5	18.8	18.8	C.H. Lee et. al, 1995	ICAM-1		37	100	P	16
GGTTGCAACTCTGAG	0.36	-16.8	-9.1	0	-11.5	20	33.3	20	26.7	C.H. Lee et. al, 1995	ICAM-1		46	100	P	15
CTGAGGTTGC	0.95	-10.8	-14.5	0	-2.6	10	40	20	30	C.H. Lee et. al, 1995	ICAM-1		55	100	P	10
GGCTGAGGTTG	0.9	-12.9	-14	0	-3.7	9.1	54.5	9.1	27.3	C.H. Lee et. al, 1995	ICAM-1		56	100	P	11
AGCGAGGCTGAG	0.79	-14.5	-12.3	-0.4	-4.6	25	50	16.7	8.3	C.H. Lee et. al, 1995	ICAM-1		60	100	P	12
AGCGAGGCTG	0.97	-12.1	-16	-0.4	-4.6	20	50	20	10	C.H. Lee et. al, 1995	ICAM-1		62	100	P	10
AGCCATAGCGAGGCTGAGGTT	0.2	-29.3	-24.2	-2.4	-8.7	23.8	38.1	19	19	C.H. Lee et. al, 1995	ICAM-1		57	100	P	21
CATAGCGAGGCTGAGGTTGC	0.39	-26.4	-19	-0.6	-5.1	20	40	20	20	C.H. Lee et. al, 1995	ICAM-1		55	100	P	20
TGGGAGCCATAGCGAG	0.55	-20.8	-24.2	-0.7	-5.1	25	43.8	18.8	12.5	C.H. Lee et. al, 1995	ICAM-1		66	100	P	16
TGGGAGCCATAGCGAGGC	0.38	-25.6	-29.3	-0.8	-6.4	22.2	44.4	22.2	11.1	C.H. Lee et. al, 1995	ICAM-1		64	100	P	18	double
GGAGCCATAGCGAGGC	0.35	-22.6	-29	-1.6	-7.2	25	43.8	25	6.3	C.H. Lee et. al, 1995	ICAM-1		64	100	P	16
AGCCATAGCGAGGC	0.64	-19	-23.7	-1.6	-7.2	28.6	35.7	28.6	7.1	C.H. Lee et. al, 1995	ICAM-1		64	100	P	14
CCATAGCGAGGC	1	-15.4	-17.6	0	-3.9	25	33.3	33.3	8.3	C.H. Lee et. al, 1995	ICAM-1		64	100	P	12
ATAGCGAGGC	1	-10.9	-12.5	0	-4.1	30	40	20	10	C.H. Lee et. al, 1995	ICAM-1		64	100	P	10
CGGGGGCTGCTGGGAGC	0.76	-27.1	-29.1	-0.8	-8.2	5.9	58.8	23.5	11.8	C.H. Lee et. al, 1995	ICAM-1		75	100	P	17
CCCCCACCACTTCCCCTCTCA	0.07	-37.4	-28.4	0	0	14.3	0	66.7	19	C.H. Lee et. al, 1995	ICAM-1		1951	100	P	21
GGGCCACTTCTTCTGTAA	0.33	-23.2	-12.7	0	-7.6	16.7	22.2	27.8	33.3	C.H. Lee et. al, 1995	ICAM-1		2053	100	P	18
CTATGGAGGGCCACTTC	0.39	-22.2	-17.2	-1.4	-7.6	17.6	29.4	29.4	23.5	C.H. Lee et. al, 1995	ICAM-1		2061	100	P	17
GCTACACATGTCTATGGAGGG	0.35	-25.5	-14.2	-0.8	-6.1	23.8	33.3	19	23.8	C.H. Lee et. al, 1995	ICAM-1		2068	100	P	21
CACATGTCTATGGAGGG	0.89	-19.3	-17.9	-0.8	-6.3	23.5	35.3	17.6	23.5	C.H. Lee et. al, 1995	ICAM-1		2068	100	P	17
GATGCTACACATGTC	0.58	-15.9	-13.4	-0.7	-6.3	26.7	20	26.7	26.7	C.H. Lee et. al, 1995	ICAM-1		2077	100	P	15
GGCAGAAATGTATGTGGGTGG	0.68	-24.7	-4.2	-0.7	-6.1	23.8	47.6	4.8	23.8	C.H. Lee et. al, 1995	ICAM-1		2509	100	P	21
ACACATACACACACACACACA	0.54	-22.7	-15.4	0	-0.7	52.4	0	42.9	4.8	C.H. Lee et. al, 1995	ICAM-1		2746	100	P	21
TTCAGGCAGTTGTTAAAATA	0.86	-18.8	-10.8	0	-3.2	35	20	10	35	S.P. Ho et. al, 1998	AT1	X62295	1145	1000	P	20
GGGTTCAGGCAGTTGTTAAA	0.29	-23.4	-6.9	0	-4	25	35	10	30	S.P. Ho et. al, 1998	AT1		1148	1000	P	20
AGAGGGTTCAGGCAGTTGTT	0.3	-25.7	-6.9	-0.3	-4.3	20	40	10	30	S.P. Ho et. al, 1998	AT1		1151	1000	P	20
AACAGAGGGTTCAGGCAGTT	0.29	-24.6	-6.9	-0.3	-4.3	30	35	15	20	S.P. Ho et. al, 1998	AT1		1154	1000	P	20	double
GTGATGGGCATGGCAGTGTC	0.29	-27.2	-25.7	-0.7	-7	15	45	15	25	S.P. Ho et. al, 1998	AT1		1112	1000	P	20
TGGTGATGGGCATGGCAGTG	0.21	-26.8	-24.9	-0.7	-5.1	15	50	10	25	S.P. Ho et. al, 1998	AT1		1114	1000	P	20
GATGGTGATGGGCATGGCAG	0.32	-26.2	-23	-0.7	-5.1	20	50	10	20	S.P. Ho et. al, 1998	AT1		1116	1000	P	20	double
TAGCTGGTGAGAATGATAAG	0.44	-18.9	-2.4	0	-5.2	35	35	5	25	S.P. Ho et. al, 1998	AT1		896	1000	P	20
GTATAGCTGGTGAGAATGAT	0.46	-20.8	0	0	-5.2	30	35	5	30	S.P. Ho et. al, 1998	AT1		899	1000	P	20
AGGGTATAGCTGGTGAGAAT	0.39	-22.6	0	0	-5.2	30	40	5	25	S.P. Ho et. al, 1998	AT1		902	1000	P	20
TAAGGGTATAGCTGGTGAGA	0.35	-22.3	0	0	0	30	40	5	25	S.P. Ho et. al, 1998	AT1		904	1000	P	20
GTCGAATTCCGAGACTCATA	0.25	-22.7	-6.2	-1.4	-6.8	30	20	25	25	S.P. Ho et. al, 1998	AT1		821	1000	P	20	double
AGCGTCGAATTCCGAGACTC	0.29	-24.9	-6.2	-1.4	-7	25	25	30	20	S.P. Ho et. al, 1998	AT1		824	1000	P	20
GGGAGCGTCGAATTCCGAGA	0.21	-26.4	-6.2	-1.4	-7.2	25	40	20	15	S.P. Ho et. al, 1998	AT1		827	1000	P	20
GGTCGATGCTGAGACACGTG	0.49	-25.2	-17	-1.4	-8.8	20	40	20	20	S.P. Ho et. al, 1998	AT1		628	1000	P	20
GCGGTCGATGCTGAGACACG	0.35	-26.6	-20.9	-1.4	-6.3	20	40	25	15	S.P. Ho et. al, 1998	AT1		630	1000	P	20
TAGCGGTCGATGCTGAGACA	0.75	-25.3	-25.6	-1.5	-6.8	25	35	20	20	S.P. Ho et. al, 1998	AT1		632	1000	P	20
GGTAGCGGTCGATGCTGAGA	0.39	-26.8	-27.5	-1.5	-6.8	20	45	15	20	S.P. Ho et. al, 1998	AT1		634	1000	P	20
ACACGTGAGAAGGAACACAC	0.51	-20.7	-11.1	-1.3	-9.3	45	25	25	5	S.P. Ho et. al, 1998	AT1		615	1000	P	20
AGACACGTGAGAAGGAACAC	0.5	-20.4	-15.7	-0.2	-9.3	45	30	20	5	S.P. Ho et. al, 1998	AT1		617	1000	P	20
GGCGTAGAGGTTGAAGCTCA	0.27	-25.5	-14.5	-1.3	-1.8	25	40	15	20	S.P. Ho et. al, 1998	AT1		594	1000	P	20
CTGGCGTAGAGGTTGAAGCT	0.41	-25.3	-14.8	-0.2	-4.8	20	40	15	25	S.P. Ho et. al, 1998	AT1		596	1000	P	20
AGAAGAGTTAAGGGCCATTT	0.46	-21.9	-14.4	0	-7.9	35	30	10	25	S.P. Ho et. al, 1998	AT1		270	1000	P	20
GCAGAAGAGTTAAGGGCCAT	0.32	-24.2	-14.4	0	-7.6	35	35	15	15	S.P. Ho et. al, 1998	AT1		272	1000	P	20
CAGCAGAAGAGTTAAGGGCC	0.37	-24.2	-14.1	0	-6.4	35	35	20	10	S.P. Ho et. al, 1998	AT1		274	1000	P	20
AACAGAGGGTTCAGGCAGTT	0.37	-24.6	-6.9	-0.3	-4.3	30	35	15	20	S.P. Ho et. al, 1998	AT1		1154	250	P	20	double
GATGGTGATGGGCATGGCAG	0.39	-26.2	-23	-0.7	-5.1	20	50	10	20	S.P. Ho et. al, 1998	AT1		1116	250	P	20	double
GTCGAATTCCGAGACTCATA	0.24	-22.7	-6.2	-1.4	-6.8	30	20	25	25	S.P. Ho et. al, 1998	AT1		821	250	P	20	double
TCTTTTGATACCATCTTCAG	0.84	-21.3	-6.1	-0.3	-3.6	20	10	25	45	S.P. Ho et. al, 1998	AT1		291	250	P	20
TGACAAATATGTAACTGTGC	0.86	-18.1	-8.8	-1	-6.3	35	20	15	30	S.P. Ho et. al, 1998	AT1		340	250	P	20
AATGACAATCACCACCAAGC	0.49	-22.1	-16.2	-0.1	-3.2	45	10	35	10	S.P. Ho et. al, 1998	AT1		411	250	P	20
AGCGATCTTACATAGGTGAT	0.77	-21.9	-6	0	-4.4	30	25	15	30	S.P. Ho et. al, 1998	AT1		564	250	P	20
TGATGCAGGTGACTTTGGCC	0.71	-26.4	-15.4	-0.7	-6.7	15	35	20	30	S.P. Ho et. al, 1998	AT1		703	250	P	20
TCAGCCAGATGATGATGCAG	0.99	-23.9	-16.6	-0.4	-6.1	30	30	20	20	S.P. Ho et. al, 1998	AT1		715	250	P	20
GGAACAAGAAGCCCAGAATA	0.46	-21.3	-14.5	0	-3.2	50	25	20	5	S.P. Ho et. al, 1998	AT1		871	250	P	20
CATAAGCCTTCTTTAGAGCT	0.58	-23	-19.5	-1	-5.7	25	15	25	35	S.P. Ho et. al, 1998	AT1		931	250	P	20
GAAGTCAGCCAAGAACAGCT	0.5	-23.5	-3.1	-0.4	-4.3	40	25	25	10	C.F. Bennett et. al, 1994	E-selectin	vXM_057446	1	50	P	20
TATAGGAGTTTTGATGTGAA	0.74	-18.4	-11.4	0	-1.5	30	30	0	40	C.F. Bennett et. al, 1994	E-selectin		18	50	P	20
CTGCTGCCTCTGTCTCAGGT	0.07	-29.6	-22.1	-0.4	-6.1	5	25	35	35	C.F. Bennett et. al, 1994	E-selectin		41	50	P	20
ACAGGATCTCTCAGGTGGGT	0.2	-26.4	-21.6	-0.1	-5	20	35	20	25	C.F. Bennett et. al, 1994	E-selectin		65	50	P	20
AATCATGACTTCAAGAGTTCT	0.53	-20.7	-8.4	-0.6	-6.8	33.3	14.3	19	33.3	C.F. Bennett et. al, 1994	E-selectin		143	50	P	21	double
TGAAGCAATCATGACTTCAAG	0.51	-19.9	-6.2	-3.5	-11.2	38.1	19	19	23.8	C.F. Bennett et. al, 1994	E-selectin		149	50	P	21	double
CCAAAGTGAGAGCTGAGAGA	0.36	-22.2	-25.6	-0.7	-5	40	35	15	10	C.F. Bennett et. al, 1994	E-selectin		175	50	P	20
CTGATTCAAGGCTTTGGCAG	0.55	-23.8	-14.5	-2	-7.2	20	30	20	30	C.F. Bennett et. al, 1994	E-selectin		1936	50	P	20
TTCCCCAGATGCACCTGTTT	0.02	-28.8	-15.3	0.4	-4.1	15	15	35	35	C.F. Bennett et. al, 1994	E-selectin		2006	50	P	20
GGGCCAGAGACCCGAGGAGA	0.46	-30.1	-18.9	-1.5	-7.6	30	45	25	0	C.F. Bennett et. al, 1994	E-selectin		2063	50	P	20
CACAATCCTTAAGAACTCTTT	0.31	-20.7	-17.5	0	-5.8	33.3	4.8	28.6	33.3	C.F. Bennett et. al, 1994	E-selectin		2617	50	P	21
GTATGGAAGATTATAATATAT	0.59	-15.7	-27.2	0	-6.2	42.9	19	0	38.1	C.F. Bennett et. al, 1994	E-selectin		2657	50	P	21
GACAATATACAAACCTTCCAT	0.65	-20.9	-2.8	0	-2.7	42.9	4.8	28.6	23.8	C.F. Bennett et. al, 1994	E-selectin		2934	50	P	21
ACGTTTGGCCTCATGGAAGT	0.35	-25.7	-13.1	-0.4	-7.2	20	30	20	30	C.F. Bennett et. al, 1994	E-selectin		2994	50	P	20
GGAATGCAAAGCACATCCAT	0.71	-22.7	-9.8	-2.6	-9.1	40	20	25	15	C.F. Bennett et. al, 1994	E-selectin		3094	50	P	20
TCCTCTCTTCCAGAGCACCC	1	-30.4	-11.3	-1.3	-5	15	10	50	25	C.F. Bennett et. al, 1994	E-selectin		3278	50	P	20
ACCTCTGCTGTTCTGATCCT	0.17	-27.6	-4.3	0	-4.3	10	15	35	40	C.F. Bennett et. al, 1994	E-selectin		3557	50	P	20
ACCACACTGGTATTTCACAC	0.67	-23.4	-23	-1.5	-5.3	30	10	35	25	C.F. Bennett et. al, 1994	E-selectin		3717	50	P	20
CAGCCAAGAACAGCT	0.5	-17.5	-3.1	-0.4	-4.3	40	20	33.3	6.7	C.H. Lee et. al, 1995	ELAM-1	vXM_057446	1	100	P	15
TGAAGTCAGCCAAGAACAGCT	0.08	-19.9	-6.2	-3.5	-11.2	38.1	19	19	23.8	C.H. Lee et. al, 1995	ELAM-1		149	100	P	21
GATGTGAAGTCAGCCAA	0.51	-19.1	-1.5	0	-3.8	35.3	29.4	17.6	17.6	C.H. Lee et. al, 1995	ELAM-1		9	100	P	17
CCCAAAGGTTTAGGCTTG	0.61	-21.8	-9.7	0	-3.7	22.2	27.8	22.2	27.8	C.H. Lee et. al, 1995	ELAM-1		120	100	P	18
TCACCCAAAGGTTTAGGCTTG	0.1	-25.8	-9.7	-1	-5.6	23.8	23.8	23.8	28.6	C.H. Lee et. al, 1995	ELAM-1		120	100	P	21
GAGTTCTTTTCACCC	0.63	-18.3	-11.5	0	-2	13.3	13.3	33.3	40	C.H. Lee et. al, 1995	ELAM-1		135	100	P	15
GACTTCAAGAGTTCT	0.82	-14.9	-10.8	-0.6	-3.8	26.7	20	20	33.3	C.H. Lee et. al, 1995	ELAM-1		143	100	P	15
AATCATGACTTCAAGAGTTCT	0.78	-20.7	-8.4	-0.6	-6.8	33.3	14.3	19	33.3	C.H. Lee et. al, 1995	ELAM-1		143	100	P	21	double
CAATCATGACTTCAAGAGTTC	0.77	-20.5	-8.4	-0.6	-6.8	33.3	14.3	23.8	28.6	C.H. Lee et. al, 1995	ELAM-1		144	100	P	21
GCAATCATGACTTCAAGAGTT	0.32	-21.9	-12.9	-0.6	-6.8	33.3	19	19	28.6	C.H. Lee et. al, 1995	ELAM-1		145	100	P	21
TGAAGCAATCATGACTTCAAG	1	-19.9	-6.2	-3.5	-11.2	38.1	19	19	23.8	C.H. Lee et. al, 1995	ELAM-1		149	100	P	21	double
CTGTGAAGCAATCATGAC	0.96	-17.9	-6.2	-0.7	-7.7	33.3	22.2	22.2	22.2	C.H. Lee et. al, 1995	ELAM-1		155	100	P	18
TGGGAGCCATAGCGAGGC	0.19	-25.6	-29.3	-0.8	-6.4	22.2	44.4	22.2	11.1	M.Y. Chiang et. al, 1991	ICAM-1	M24283	64	70	P	18	double
GAGGAGCTCAGCGTCGACTG	1	-26.9	-22.6	-0.4	-9.2	20	40	25	15	M.Y. Chiang et. al, 1991	ICAM-1		21	70	P	20	double
GACACTCAATAAATAGCTGGT	0.1	-21	-26.3	0	-4.8	38.1	19	19	23.8	M.Y. Chiang et. al, 1991	ICAM-1		2191	70	P	21
GAGGCTGAGGTGGGAGGA	0.5	-24.5	-16.3	0	-3.7	22.2	61.1	5.6	11.1	M.Y. Chiang et. al, 1991	ICAM-1		2853	70	P	18
CGATGGGCAGTGGGAAAG	0.25	-21.3	-15.7	0	-4.4	27.8	50	11.1	11.1	M.Y. Chiang et. al, 1991	ICAM-1		1378	70	P	18
GGGCGCGTGATCCTTATAGC	1	-28	-14.1	0	-8.4	15	35	25	25	M.Y. Chiang et. al, 1991	ICAM-1		1	70	P	20
TGCCCATCAGGGCAGTTTGA	0.4	-28.5	-14.9	-5.2	-11.9	20	30	25	25	M.Y. Chiang et. al, 1991	ICAM-1		351	70	P	20
CCTGTCCCGGGATAGGTTCA	0.1	-29.6	-15	-0.8	-16.8	15	30	30	25	M.Y. Chiang et. al, 1991	ICAM-1		1668	70	P	20
CCCCCACCACTTCCCCTCTC	0	-35.8	-28.4	0	0	10	0	70	20	M.Y. Chiang et. al, 1991	ICAM-1		1952	70	P	20
TTGAGAAAGCTTTATTAACT	0.8	-16.7	-6.7	0	-8.7	35	15	10	40	M.Y. Chiang et. al, 1991	ICAM-1		2979	70	P	20
CCCCAACCACCTCTTGCTCC	0.39	-32.5	-16.5	0	-3.6	15	5	60	20	N.M. Dean et. al, 1994	PKC-alpha	X52479	1	1000	P	20
AAAACGTCAGCCATGGTCCC	0.39	-26.5	-10.5	0	-8.4	30	20	35	15	N.M. Dean et. al, 1994	PKC-alpha		22	1000	P	20
CCCGGGAAAACGTCAGCCAT	0.52	-27.5	-11	-0.1	-9.2	30	25	35	10	N.M. Dean et. al, 1994	PKC-alpha		28	1000	P	20
GTCAGCCATGGTCCCCCCCC	0.46	-37.6	-10.5	-0.1	-8.3	10	20	55	15	N.M. Dean et. al, 1994	PKC-alpha		17	1000	P	20
CGCCGTGGAGTCGTTGCCCG	0.54	-32.7	-8.8	0	-4.7	5	40	35	20	N.M. Dean et. al, 1994	PKC-alpha		44	1000	P	20
CTGCCTCAGCGCCCCTTTGC	0.47	-34	-23.5	-1.4	-7.6	5	20	50	25	N.M. Dean et. al, 1994	PKC-alpha		92	1000	P	20
GCAGAGGCTGGGGACATTGA	0.81	-26.8	-20	-0.5	-4.8	25	45	15	15	N.M. Dean et. al, 1994	PKC-alpha		461	1000	P	20
ATGGGGTGCACAAACTGGGG	0.94	-25.5	-21	0	-9	25	45	15	15	N.M. Dean et. al, 1994	PKC-alpha		2008	1000	P	20
TCAAATGGAGGCTGCCCGGC	0.66	-29	-12.3	-0.9	-9.2	20	35	30	15	N.M. Dean et. al, 1994	PKC-alpha		1624	1000	P	20
GTTCTCGCTGGTGAGTTTCA	0.52	-26	-9.8	-1.5	-8.3	10	30	20	40	N.M. Dean et. al, 1994	PKC-alpha		2044	1000	P	20
GGATTCACTTCCACTGCGGG	0.82	-27.4	-13.6	-0.4	-5.2	15	30	30	25	N.M. Dean et. al, 1994	PKC-alpha		2090	1000	P	20
GAGACCCTGAACAGTTGATC	0.61	-23.4	-11.7	0	-5.1	30	25	25	20	N.M. Dean et. al, 1994	PKC-alpha		2192	1000	P	20
GGGCTGGGGAGGTGTTTGTT	0.95	-28.4	-19.4	0	-3.7	5	55	5	35	N.M. Dean et. al, 1994	PKC-alpha		2061	1000	P	20
CACTGCGGGGAGGGCTGGGG	1	-31.3	-33.9	-0.4	-5.1	10	60	20	10	N.M. Dean et. al, 1994	PKC-alpha		2079	1000	P	20
AGCCGTGGCCTTAAAATTTT	0.84	-23.7	-19.2	0	-8.8	25	20	20	35	N.M. Dean et. al, 1994	PKC-alpha		2118	1000	P	20
ATTTTCAGGCCTCCATATGG	0.82	-25.3	-20.2	-0.3	-9.2	20	20	25	35	N.M. Dean et. al, 1994	PKC-alpha		2149	1000	P	20
AAGAGAGAGACCCTGAACAG	0.62	-21.6	-11.3	0	-4.7	45	30	20	5	N.M. Dean et. al, 1994	PKC-alpha		2198	1000	P	20
GATAATGTTCTTGGTTGTAA	0.85	-19	-11.7	0	-1.6	25	25	5	45	N.M. Dean et. al, 1994	PKC-alpha		2216	1000	P	20
TGGAATCAGACACAAGCCGT	0.89	-23.7	-3.9	0	-3.4	35	25	25	15	N.M. Dean et. al, 1994	PKC-alpha		2132	1000	R	20
CTTTCATATTCTTCTTGGAG	0.9	-20.6	-17.7	0	-2.7	15	10	55	20	L. Miraglia et. al, 1996	IL-1	XM002686	340	400	R	20
TCTTCAGAGGGTGCGTCTAC	0.9	-25.7	-7.3	0	-4.1	15	15	20	50	L. Miraglia et. al, 1996	IL-1		270	400	R	20
CTTGGAGAAGGCCTTGTCTT	0.9	-25.3	-16.9	-0.2	-12.4	15	30	25	30	L. Miraglia et. al, 1996	IL-1		327	400	R	20
AGTAACACTTTCATATTCTT	0.9	-18.7	-13.6	0	-2.9	15	30	20	35	L. Miraglia et. al, 1996	IL-1		347	400	R	20
GAAACAAATAAGTCTGAGTA	0.9	-15.7	-5.7	0	-2.9	30	5	20	45	L. Miraglia et. al, 1996	IL-1		363	400	R	20
AGTCCTCCGTCTCCTGCAAC	0.9	-29.5	-18.3	0	-4.9	50	20	10	20	L. Miraglia et. al, 1996	IL-1		752	400	R	20
TACCCGAGAGGCACGTGAGC	0.9	-28.2	-23.8	-1.1	-12.2	15	15	45	25	L. Miraglia et. al, 1996	IL-1		2042	400	R	20
TCTGGCATTTTCTCATAGTC	0.9	-23	-10.3	0	-4	25	35	30	10	L. Miraglia et. al, 1996	IL-1		1835	400	R	20
CCCTTCCATAAATGAACAGC	0.9	-23	-11.9	0	-3.5	15	15	25	45	L. Miraglia et. al, 1996	IL-1		2687	400	R	20
AACTTCTCCATGCTACCCGA	0.9	-26.9	-17.2	0	-4.2	10	35	25	30	L. Miraglia et. al, 1996	IL-1		2055	400	R	20
GCAACGCCATAAGACAGGAG	0.9	-23.6	-14.9	0	-3.5	25	10	40	25	L. Miraglia et. al, 1996	IL-1		2095	400	R	20
CATAACCTGGCCTGCAACGC	0.9	-27.3	-15.7	0	-7.2	40	30	25	5	L. Miraglia et. al, 1996	IL-1		2139	400	R	20
CATTCCATGAACTCTGCAAG	0.9	-22	-15.6	0	-4.9	30	15	30	25	L. Miraglia et. al, 1996	IL-1		1618	400	R	20
CACTGCAACCTCCGTCTCCC	0.54	-30.8	-32.3	0	-4.9	35	10	35	20	L. Miraglia et. al, 1996	IL-1		2108	400	R	20
CCCTTGGGCTGTGGATGACT	0.3	-28.8	-28.4	-0.1	-5.3	25	20	40	15	L. Miraglia et. al, 1996	IL-1		2687	400	R	20
GCGGGATGACAGAAGAGCGG	0.9	-25.4	-25	0	-4.2	10	35	25	30	L. Miraglia et. al, 1996	IL-1		3176	400	R	20
GCCACCACAGCCTCTCCCTC	0.42	-34	-36.8	0	-3.2	30	50	15	5	L. Miraglia et. al, 1996	IL-1		3614	400	R	20
CGTGCCAGTGTGGAGTGAGG	0.23	-27.7	-7.8	-1	-4.4	15	10	60	15	L. Miraglia et. al, 1996	IL-1		3888	400	R	20
TGTGTCCTGCAATCGGTGGC	0.1	-28.1	-15.5	0	-4.9	15	50	15	20	L. Miraglia et. al, 1996	IL-1		4121	400	R	20
GCAAAGCGGGCCCAGGAGAA	0.3	-28.3	-25.3	0	-11	10	35	25	30	L. Miraglia et. al, 1996	IL-1		4302	400	R	20
CCTCCACCCACGCTTATCCA	0.29	-31.5	-24.6	0	-3.3	35	40	25	0	L. Miraglia et. al, 1996	IL-1		4642	400	R	20
AGTCAAAGGAAGTTCACGGG	0.9	-21.8	-19.7	0	-6.7	20	5	55	20	L. Miraglia et. al, 1996	IL-1		4743	400	R	20
TGATCCGTGATGCATGCTGT	0.9	-26	-8	0	-9.7	35	35	15	15	L. Miraglia et. al, 1996	IL-1		5110	400	P	20
GCCAGTGAGGCCCG	0.35	-22.7	-13.2	-1.9	-6.8	15	30	20	35	C.H. Lee et. al, 1995	VCAM-1	NM_001078	15	100	P	14
CCTGAAGCCAGTGAGG	0.61	-20.7	-17	-0.9	-4.3	14.3	42.9	35.7	7.1	C.H. Lee et. al, 1995	VCAM-1		19	100	P	16
GGTATTCAGCTCCTGAAG	0.69	-21.4	-16	-2.4	-7.8	25	37.5	25	12.5	C.H. Lee et. al, 1995	VCAM-1		28	100	P	18
GCCTGGGAGGGTATTCAGCTC	0.3	-30.2	-33	-0.8	-5.9	22.2	27.8	22.2	27.8	C.H. Lee et. al, 1995	VCAM-1		34	100	P	21
CCTGGGAGGGTATTC	0.39	-19.2	-17.7	-0.1	-3.6	14.3	38.1	23.8	23.8	C.H. Lee et. al, 1995	VCAM-1		39	100	P	15
ACCTGTGTGTGCCTGGGAGGG	0.25	-31.7	-20.7	-0.8	-4.9	13.3	40	20	26.7	C.H. Lee et. al, 1995	VCAM-1		44	100	P	21
TTTGTGTCCCACCTG	0.1	-20.3	-11.8	-0.6	-3.9	9.5	47.6	19	23.8	C.H. Lee et. al, 1995	VCAM-1		60	100	P	15
CCCTTATTTGTGTCCC	0.37	-22.1	-19.2	0	-0.5	6.7	20	33.3	40	C.H. Lee et. al, 1995	VCAM-1		65	100	P	16
AACCCTTATTTGTGTCCCACC	0.09	-29	-14.1	-0.6	-3.9	6.3	12.5	37.5	43.8	C.H. Lee et. al, 1995	VCAM-1		62	100	P	21
GGTTCCAAAACCCTT	0.42	-18.2	-8.3	-1.7	-5	19	9.5	38.1	33.3	C.H. Lee et. al, 1995	VCAM-1		76	100	P	15
CGTGATGAGAAAATAGTGGTT	0.49	-20	-14.1	0	-1.8	26.7	13.3	33.3	26.7	C.H. Lee et. al, 1995	VCAM-1		87	100	P	21
CCCAGGCATTTTAAGTTGCTG	0.33	-26.6	-19.9	-0.7	-5.7	33.3	33.3	4.8	28.6	C.H. Lee et. al, 1995	VCAM-1		109	100	P	21
CCCAGGCATTTTAAG	0.78	-19.8	-18.6	0	-2.4	19	23.8	23.8	33.3	C.H. Lee et. al, 1995	VCAM-1		1347	100	P	15
CGACCATCTTCCCAGGCATTT	0.2	-29.6	-24.5	0	-4	20	6.7	53.3	20	C.H. Lee et. al, 1995	VCAM-1		119	100	P	21
CATCTTCCCAGGCAT	0.45	-20.4	-17.8	0	-4	19	14.3	38.1	28.6	C.H. Lee et. al, 1995	VCAM-1		121	100	P	15
ACGACCATCTTCCC	0.51	-18.9	-19.6	0	-3.5	20	13.3	40	26.7	C.H. Lee et. al, 1995	VCAM-1		127	100	P	14
CATCTCGATTTCTGG	0.47	-16	-18	0	-4.5	21.4	7.1	50	21.4	C.H. Lee et. al, 1995	VCAM-1		1339	100	P	15
CCACCACTCATCTCG	0.26	-17.2	-19.9	0	-3.3	13.3	20	26.7	40	C.H. Lee et. al, 1995	VCAM-1		115	100	P	15
CACGAGGCCACCACTCATCTC	0.05	-29.7	-16.7	-1	-6.9	26.7	20	26.7	26.7	C.H. Lee et. al, 1995	VCAM-1		1348	100	P	21
CGAGGCCACCACTC	0.16	-20.1	-12	-0.3	-7.7	23.8	14.3	47.6	14.3	C.H. Lee et. al, 1995	VCAM-1		1353	100	P	14
CCCATTCACGAGGCCACC	0.11	-27.6	-20.1	0	-7.7	21.4	21.4	50	7.1	C.H. Lee et. al, 1995	VCAM-1		1357	100	P	18
CTTTGACTTCTTGCTCACAGC	0.07	-25.7	-19.3	-0.8	-3.9	22.2	16.7	50	11.1	C.H. Lee et. al, 1995	VCAM-1		2488	100	P	21
CTCTCATCTTGATGGC	0.55	-18.7	-17.9	-1.5	-6.9	14.3	14.3	33.3	38.1	C.H. Lee et. al, 1995	VCAM-1		2538	100	P	16
AACTCCTCCAGTTCTCTCATC	0.12	-27.1	-14.8	-0.6	-3.3	12.5	18.8	31.3	37.5	C.H. Lee et. al, 1995	VCAM-1		2546	100	P	21
CCTCCAGTTCTCTC	0.32	-18.9	-9.5	0	-1.4	19	4.8	42.9	33.3	C.H. Lee et. al, 1995	VCAM-1		2549	100	P	14
CAGATCAAGGAACTCCTC	0.55	-19.8	-10.7	-0.6	-6.9	7.1	7.1	50	35.7	C.H. Lee et. al, 1995	VCAM-1		2559	100	P	18
TTTAAGCAATCTTGCTATGGC	0.81	-22.7	-17.4	-2.3	-10	33.3	16.7	33.3	16.7	C.H. Lee et. al, 1995	VCAM-1		2620	100	R	21