Variant report

Variant	rs638921
Chromosome Location	chr6:80980648-80980649
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:80979089..80982797-chr6:80991689..80993882,3	K562	blood:

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs1040593	0.83[ASN][1000 genomes]
rs1179571	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12525046	1.00[ASN][1000 genomes]
rs12526876	1.00[ASN][1000 genomes]
rs12527244	1.00[ASN][1000 genomes]
rs12527712	1.00[ASN][1000 genomes]
rs12530290	1.00[ASN][1000 genomes]
rs16891532	1.00[ASN][1000 genomes]
rs16891545	1.00[ASN][1000 genomes]
rs4706829	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4706830	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55755254	1.00[ASN][1000 genomes]
rs57913486	1.00[ASN][1000 genomes]
rs57985210	1.00[ASN][1000 genomes]
rs584372	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs585506	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs587999	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs588009	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs590686	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs595494	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs598234	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59973779	1.00[ASN][1000 genomes]
rs604732	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs610946	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs612208	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs613577	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs623085	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs627968	0.88[EUR][1000 genomes]
rs631314	0.82[EUR][1000 genomes]
rs631367	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs634499	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs636499	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs640568	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs641229	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs642943	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs644666	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6454149	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs646369	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs649148	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs651065	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs652576	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs66518170	1.00[ASN][1000 genomes]
rs66560352	1.00[ASN][1000 genomes]
rs66606872	0.86[ASN][1000 genomes]
rs669420	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs670119	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs670390	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs671614	0.88[EUR][1000 genomes]
rs67379633	1.00[ASN][1000 genomes]
rs67456645	1.00[ASN][1000 genomes]
rs67597629	1.00[ASN][1000 genomes]
rs67632695	1.00[ASN][1000 genomes]
rs677134	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67851250	1.00[ASN][1000 genomes]
rs67988458	1.00[ASN][1000 genomes]
rs685902	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs687702	0.82[EUR][1000 genomes]
rs688442	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6906403	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6908084	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6920430	0.83[ASN][1000 genomes]
rs6924011	1.00[ASN][1000 genomes]
rs723308	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72892417	1.00[ASN][1000 genomes]
rs72892426	1.00[ASN][1000 genomes]
rs72892441	1.00[ASN][1000 genomes]
rs72892456	1.00[ASN][1000 genomes]
rs72892458	1.00[ASN][1000 genomes]
rs72908809	1.00[ASN][1000 genomes]
rs72908854	1.00[ASN][1000 genomes]
rs73479994	1.00[ASN][1000 genomes]
rs764442	1.00[ASN][1000 genomes]
rs7757610	1.00[ASN][1000 genomes]
rs7771726	1.00[ASN][1000 genomes]
rs7772483	1.00[ASN][1000 genomes]
rs806781	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs806839	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs806844	0.83[ASN][1000 genomes]
rs806846	0.83[ASN][1000 genomes]
rs806850	0.83[ASN][1000 genomes]
rs811567	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs932463	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9443739	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9688524	1.00[ASN][1000 genomes]
rs9688535	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830708	chr6:80844283-80996876	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1034096	chr6:80856135-81150170	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv886310	chr6:80880138-81025879	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv932996	chr6:80880896-81134991	Flanking Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
5	nsv497995	chr6:80883701-81134991	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv1033452	chr6:80888667-81000213	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80944000-80982800	Weak transcription	Pancreas	Pancrea
2	chr6:80960600-80997400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr6:80964800-81002600	Weak transcription	Liver	Liver
4	chr6:80968400-81006800	Weak transcription	Psoas Muscle	Psoas
5	chr6:80975200-80985000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:80977000-80983600	Weak transcription	HSMM	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links