Variant report

Variant	rs6502619
Chromosome Location	chr17:17779704-17779705
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:17774108..17776065-chr17:17778403..17780071,2	K562	blood:
2	chr17:17772782..17775261-chr17:17777094..17780036,2	K562	blood:
3	chr17:17778338..17781042-chr17:17785624..17789074,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000175662	Chromatin interaction

Extended variants
information (count: 157 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:135)

rs_ID	r²[population]
rs10048206	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs1052299	0.83[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11078400	0.91[CEU][hapmap];0.86[EUR][1000 genomes]
rs11078403	0.93[EUR][1000 genomes]
rs11078404	0.90[EUR][1000 genomes]
rs11078405	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11078406	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs11078407	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1108648	0.81[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11650649	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11650890	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11652144	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11652881	0.82[JPT][hapmap]
rs11656665	0.82[JPT][hapmap];0.82[AMR][1000 genomes]
rs11656840	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11657074	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11657130	0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11657423	1.00[CHB][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes]
rs11657773	0.81[EUR][1000 genomes]
rs11657845	0.82[EUR][1000 genomes]
rs11658309	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11869536	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11871899	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12452219	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12452254	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12600546	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs12603148	0.90[EUR][1000 genomes]
rs12936037	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12941039	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12943500	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12946746	0.87[AMR][1000 genomes]
rs12953299	0.80[CEU][hapmap];1.00[CHB][hapmap]
rs16960744	0.83[CEU][hapmap];0.81[AMR][1000 genomes]
rs1889014	1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1889018	1.00[CHB][hapmap];0.82[JPT][hapmap];0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2236513	0.83[CEU][hapmap];0.82[JPT][hapmap]
rs2350976	0.82[JPT][hapmap]
rs2350977	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28428991	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2955371	0.91[CEU][hapmap];0.82[JPT][hapmap]
rs2955382	0.82[CEU][hapmap];1.00[JPT][hapmap]
rs3183702	0.87[CEU][hapmap];0.82[JPT][hapmap]
rs35451946	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3744113	0.81[EUR][1000 genomes]
rs3744115	1.00[CHB][hapmap];0.82[JPT][hapmap];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3818717	0.82[JPT][hapmap]
rs4077198	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4077828	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4244602	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4257260	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs4321247	0.88[EUR][1000 genomes]
rs4341796	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4343339	0.89[EUR][1000 genomes]
rs4413022	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs4414547	0.90[EUR][1000 genomes]
rs4470201	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4534911	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4553680	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4616340	0.90[EUR][1000 genomes]
rs4924821	0.81[AMR][1000 genomes]
rs4924822	0.82[JPT][hapmap]
rs4924823	0.91[CEU][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4925120	0.83[CEU][hapmap]
rs4925123	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4925125	0.95[CEU][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4925126	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4925129	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4925130	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5002487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62064156	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62064158	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6502618	0.88[ASN][1000 genomes]
rs6502622	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6502624	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6502625	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6502626	0.91[EUR][1000 genomes]
rs6502627	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs6502629	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs66531105	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs67253360	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7207043	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7207395	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7208190	0.88[EUR][1000 genomes]
rs7213225	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs7214002	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs7214536	0.91[EUR][1000 genomes]
rs7222480	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7224815	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7359509	1.00[CHB][hapmap];0.82[JPT][hapmap];0.87[AMR][1000 genomes]
rs7501812	1.00[CHB][hapmap];0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs7503334	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7503747	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs8065416	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs8065497	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8065563	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8065970	0.90[EUR][1000 genomes]
rs8066982	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs8068820	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs8070128	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8070624	0.87[ASN][1000 genomes]
rs8070722	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8070748	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs8073001	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8075965	0.87[EUR][1000 genomes]
rs8076747	0.88[EUR][1000 genomes]
rs8077338	0.91[ASN][1000 genomes]
rs8077530	0.88[EUR][1000 genomes]
rs8078105	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs8078138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8078583	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8078756	0.88[ASN][1000 genomes]
rs8079321	0.91[CEU][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs8080061	0.91[CEU][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs8080823	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs950966	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9635697	0.90[EUR][1000 genomes]
rs9635698	0.89[EUR][1000 genomes]
rs9890341	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9891957	1.00[CHB][hapmap];0.82[JPT][hapmap];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9895335	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9895750	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9899634	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs9902941	0.82[JPT][hapmap]
rs9904163	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9905284	0.90[EUR][1000 genomes]
rs9906673	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9907246	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9907287	0.91[CEU][hapmap];0.87[EUR][1000 genomes]
rs9908017	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9908299	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9908832	0.88[EUR][1000 genomes]
rs9911281	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9912895	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9913724	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9915248	0.83[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv907748	chr17:17412032-17782404	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	nsv1065270	chr17:17430116-17823086	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv543236	chr17:17430116-17823086	Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
4	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
5	nsv907754	chr17:17573539-17782404	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
6	nsv1061126	chr17:17578826-17803194	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
7	nsv543238	chr17:17578826-17803194	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
8	nsv1058884	chr17:17594370-17803194	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
9	nsv543240	chr17:17594370-17803194	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
10	nsv1064176	chr17:17596222-17803194	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
11	nsv543242	chr17:17596222-17803194	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
12	nsv907758	chr17:17619859-17782404	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
13	nsv907759	chr17:17619859-17802478	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
14	nsv1059949	chr17:17632590-17803194	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
15	nsv543244	chr17:17632590-17803194	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
16	nsv907760	chr17:17649423-17782404	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
17	nsv907761	chr17:17649423-17802478	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
18	nsv916653	chr17:17651916-18454952	Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
19	nsv907762	chr17:17668071-17802478	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
20	nsv907765	chr17:17682484-17802478	Active TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
21	nsv907766	chr17:17682484-17957348	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
22	nsv533142	chr17:17691726-18236686	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6502619	SREBF1	cis	Whole Blood	GTEx

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17756800-17789600	Weak transcription	Small Intestine	intestine
2	chr17:17758800-17780200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr17:17764200-17803000	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr17:17764400-17799600	Weak transcription	A549	lung
5	chr17:17767600-17782000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr17:17767600-17782000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr17:17767600-17807400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr17:17768400-17781400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr17:17768400-17792200	Weak transcription	GM12878-XiMat	blood
10	chr17:17769200-17789400	Strong transcription	Primary T cells fromperipheralblood	blood
11	chr17:17769200-17804600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr17:17769400-17792400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr17:17769600-17795200	Strong transcription	Primary T cells from cord blood	blood
14	chr17:17770000-17779800	Weak transcription	Stomach Mucosa	stomach
15	chr17:17772000-17779800	Weak transcription	Aorta	Aorta
16	chr17:17772000-17780000	Weak transcription	Primary B cells from peripheral blood	blood
17	chr17:17772000-17780000	Weak transcription	Colonic Mucosa	Colon
18	chr17:17772200-17783600	Weak transcription	HepG2	liver
19	chr17:17772600-17781400	Weak transcription	Dnd41	blood
20	chr17:17772800-17779800	Weak transcription	Ovary	ovary
21	chr17:17773600-17779800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr17:17773800-17780600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr17:17774000-17780000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr17:17774200-17780800	Weak transcription	Primary hematopoietic stem cells	blood
25	chr17:17775200-17783000	Genic enhancers	Fetal Muscle Leg	muscle
26	chr17:17775400-17780600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr17:17775600-17784000	Genic enhancers	Fetal Stomach	stomach
28	chr17:17775800-17782000	Genic enhancers	Brain Cingulate Gyrus	brain
29	chr17:17776000-17779800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr17:17776200-17780200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr17:17776200-17783600	Genic enhancers	Fetal Muscle Trunk	muscle
32	chr17:17776400-17803200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr17:17777200-17779800	Weak transcription	Brain Substantia Nigra	brain
34	chr17:17777200-17779800	Weak transcription	Spleen	Spleen
35	chr17:17777200-17780000	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr17:17778000-17779800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr17:17778000-17780000	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr17:17778000-17780200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr17:17778000-17780600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr17:17778000-17780600	Strong transcription	HSMM	muscle
41	chr17:17778000-17781400	Strong transcription	Sigmoid Colon	Sigmoid Colon
42	chr17:17778000-17781800	Enhancers	Fetal Lung	lung
43	chr17:17778000-17781800	Enhancers	Left Ventricle	heart
44	chr17:17778000-17781800	Enhancers	Right Ventricle	heart
45	chr17:17778000-17782400	Genic enhancers	NHLF	lung
46	chr17:17778000-17783800	Genic enhancers	Duodenum Smooth Muscle	Duodenum
47	chr17:17778000-17788600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr17:17778000-17789000	Strong transcription	Primary monocytes fromperipheralblood	blood
49	chr17:17778000-17789400	Strong transcription	Thymus	Thymus
50	chr17:17778200-17779800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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