Variant report

Variant	rs9864170
Chromosome Location	chr3:85610908-85610909
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 227 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:203)

rs_ID	r²[population]
rs10511075	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[ASN][1000 genomes]
rs10511076	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs10511081	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs10511083	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs10511085	0.85[CHB][hapmap];0.86[YRI][hapmap]
rs10865609	0.85[TSI][hapmap]
rs10865610	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs11127892	0.82[CHB][hapmap]
rs11127896	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs11127899	0.81[ASN][1000 genomes]
rs11127900	0.81[ASN][1000 genomes]
rs11714549	0.82[TSI][hapmap]
rs11919099	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs12054398	0.82[CHB][hapmap]
rs12485813	0.82[CHB][hapmap]
rs12486274	0.82[CHB][hapmap]
rs12488750	0.82[CHB][hapmap]
rs12493645	0.82[CHB][hapmap]
rs12494446	0.93[YRI][hapmap]
rs12634226	0.82[CHB][hapmap]
rs12637214	0.82[CHB][hapmap]
rs12637236	0.82[CHB][hapmap]
rs12638040	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs12638154	0.82[CHB][hapmap]
rs12638296	0.82[CHB][hapmap]
rs12638482	0.85[CHB][hapmap]
rs12639409	0.82[CHB][hapmap]
rs12639564	0.93[YRI][hapmap]
rs1375545	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1375551	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1375554	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1375555	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1375557	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1375562	0.85[TSI][hapmap]
rs1375566	0.85[YRI][hapmap]
rs1449372	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1449373	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1449378	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1449379	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1449380	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1449381	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1449382	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1449390	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs1449391	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs1449403	0.85[TSI][hapmap]
rs1449405	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1449409	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1463203	0.81[ASN][1000 genomes]
rs1463204	0.81[ASN][1000 genomes]
rs1463205	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1463206	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1463207	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1463208	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1465716	0.82[TSI][hapmap]
rs1470635	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs1530738	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1530739	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1530740	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.80[LWK][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1542248	0.85[CHB][hapmap];0.95[CHD][hapmap];0.86[YRI][hapmap]
rs1549979	0.85[CHB][hapmap];0.90[CHD][hapmap]
rs1551045	0.81[ASN][1000 genomes]
rs1551046	0.81[ASN][1000 genomes]
rs1551047	0.81[AFR][1000 genomes]
rs1551048	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1597315	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs17022915	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17023022	0.82[CHB][hapmap]
rs17456763	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.80[LWK][hapmap];0.93[YRI][hapmap]
rs17456820	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap]
rs17457050	0.81[ASN][1000 genomes]
rs17457217	0.81[ASN][1000 genomes]
rs17457377	0.81[ASN][1000 genomes]
rs17457426	0.81[ASN][1000 genomes]
rs17457454	0.81[ASN][1000 genomes]
rs17457642	0.81[ASN][1000 genomes]
rs17457669	0.81[ASN][1000 genomes]
rs17459563	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs17460701	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs17515586	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17516256	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17516284	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs17516346	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.80[LWK][hapmap];0.93[YRI][hapmap]
rs17516470	0.81[ASN][1000 genomes]
rs17516504	0.81[ASN][1000 genomes]
rs17516546	0.81[ASN][1000 genomes]
rs17516580	0.81[ASN][1000 genomes]
rs17516683	0.81[ASN][1000 genomes]
rs17516857	0.81[ASN][1000 genomes]
rs17517080	0.81[ASN][1000 genomes]
rs17517121	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.80[LWK][hapmap];0.93[YRI][hapmap];0.81[ASN][1000 genomes]
rs17517142	0.81[ASN][1000 genomes]
rs17517238	0.81[ASN][1000 genomes]
rs17517273	0.81[ASN][1000 genomes]
rs17518584	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.80[LWK][hapmap];0.93[YRI][hapmap]
rs17519241	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs17519262	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1865250	0.85[CHB][hapmap]
rs1865251	0.85[CHB][hapmap]
rs1865252	0.85[CHB][hapmap]
rs1868532	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs1900914	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1900918	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.81[ASN][1000 genomes]
rs1947221	0.93[YRI][hapmap]
rs1991872	0.85[CHB][hapmap]
rs2017293	0.81[TSI][hapmap]
rs2029130	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap]
rs2029132	0.93[YRI][hapmap]
rs2029133	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs2053108	0.85[CHB][hapmap];0.90[CHD][hapmap]
rs2069123	0.85[CHB][hapmap];0.86[YRI][hapmap]
rs2082556	0.85[CHB][hapmap];0.90[CHD][hapmap]
rs2117153	0.85[CHB][hapmap];0.89[CHD][hapmap]
rs2122233	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs2122234	0.81[ASN][1000 genomes]
rs2122235	0.81[ASN][1000 genomes]
rs2167043	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs2167044	1.00[CHB][hapmap];0.88[JPT][hapmap];0.92[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs2167045	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs2167046	0.81[ASN][1000 genomes]
rs2167047	0.92[YRI][hapmap];0.81[ASN][1000 genomes]
rs2326309	0.85[CHB][hapmap];0.90[CHD][hapmap]
rs2326320	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs28655875	0.85[CHB][hapmap];0.90[CHD][hapmap]
rs34305569	0.81[ASN][1000 genomes]
rs35438712	0.81[ASN][1000 genomes]
rs35827242	0.85[CHB][hapmap];0.84[CHD][hapmap]
rs4441668	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs4502590	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4603966	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4856271	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[ASN][1000 genomes]
rs4856572	0.85[CHB][hapmap];0.90[CHD][hapmap]
rs4856582	0.85[TSI][hapmap]
rs4856588	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs4856589	0.81[ASN][1000 genomes]
rs4856590	0.90[JPT][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes]
rs4856596	1.00[CHB][hapmap];0.89[JPT][hapmap];0.93[YRI][hapmap]
rs56779213	0.81[ASN][1000 genomes]
rs57756567	0.81[ASN][1000 genomes]
rs58796643	0.80[ASN][1000 genomes]
rs58919842	0.81[ASN][1000 genomes]
rs59073108	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs59770976	0.81[ASN][1000 genomes]
rs61586601	0.81[ASN][1000 genomes]
rs62250467	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs62250468	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs62252512	0.81[ASN][1000 genomes]
rs62252513	0.81[ASN][1000 genomes]
rs62252516	0.81[ASN][1000 genomes]
rs62252518	0.81[ASN][1000 genomes]
rs62252519	0.81[ASN][1000 genomes]
rs62253964	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs62253965	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs6549036	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs6549039	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs6549040	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap]
rs6549041	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs6549043	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs66625173	0.81[ASN][1000 genomes]
rs66781790	0.81[ASN][1000 genomes]
rs66922686	0.81[ASN][1000 genomes]
rs67544605	0.81[ASN][1000 genomes]
rs6762535	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs6762733	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs6765881	0.81[ASN][1000 genomes]
rs6765991	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs6766493	0.81[ASN][1000 genomes]
rs6766690	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs6767245	0.82[CHB][hapmap]
rs6767256	0.82[CHB][hapmap]
rs6767921	0.82[CHB][hapmap]
rs6777456	0.81[ASN][1000 genomes]
rs6777458	0.81[ASN][1000 genomes]
rs6778223	0.85[TSI][hapmap]
rs6779501	0.81[ASN][1000 genomes]
rs6780346	0.82[ASN][1000 genomes]
rs6780968	0.85[CHB][hapmap]
rs6781515	0.82[TSI][hapmap]
rs6788098	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs6790090	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[ASN][1000 genomes]
rs6790699	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs6791938	0.82[CHB][hapmap]
rs6794866	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs6801823	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs6804845	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs724304	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs72615727	0.81[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs7609594	0.85[CHB][hapmap];0.90[CHD][hapmap]
rs7614148	0.85[CHB][hapmap];0.86[YRI][hapmap]
rs7616458	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs7617356	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs7618429	1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[YRI][hapmap]
rs7620313	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.81[ASN][1000 genomes]
rs7623947	0.85[TSI][hapmap]
rs7634761	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs7653790	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs892365	0.82[TSI][hapmap]
rs919874	0.82[CHB][hapmap]
rs956281	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs9824071	0.82[TSI][hapmap]
rs9824840	0.82[TSI][hapmap]
rs993136	0.85[CHB][hapmap];0.90[CHD][hapmap]
rs993137	0.85[CHB][hapmap];0.90[CHD][hapmap]
rs993716	0.85[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3419993	chr3:85030343-85663403	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
2	esv2753915	chr3:85071410-85624810	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1002238	chr3:85357855-85719373	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
4	nsv536619	chr3:85357855-85719373	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
5	nsv590905	chr3:85438564-85797093	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv998829	chr3:85449960-85641099	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv536622	chr3:85449960-85641099	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv526621	chr3:85470642-85667683	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv1009927	chr3:85497666-85669155	Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1010541	chr3:85505839-85870597	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv536625	chr3:85505839-85870597	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv1002139	chr3:85534559-85630146	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv1006433	chr3:85535783-85631667	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv590906	chr3:85539816-85626054	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv1008269	chr3:85544536-85617198	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv536627	chr3:85544536-85617198	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv527642	chr3:85551353-85619451	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv1007503	chr3:85558527-85617198	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv1013950	chr3:85561009-85631527	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv536628	chr3:85561009-85631527	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
21	nsv1006141	chr3:85577197-85619079	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv1006360	chr3:85597755-85683081	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
23	nsv536629	chr3:85597755-85683081	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv1011376	chr3:85599411-85657771	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85609200-85611000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:85610400-85613000	Weak transcription	Muscle Satellite Cultured Cells	--

The 2.0 version of rSNPBase

Variant report

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