Variant report

Variant	rs7639512
Chromosome Location	chr3:140444632-140444633
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:140442579..140445613-chr3:140449550..140453378,3	K562	blood:

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs1389812	0.90[CEU][hapmap]
rs17352519	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55726121	0.82[EUR][1000 genomes]
rs58008037	0.81[EUR][1000 genomes]
rs58956782	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60130391	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61491602	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6439940	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6439941	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6439942	0.82[EUR][1000 genomes]
rs6780472	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6784484	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6798040	0.82[EUR][1000 genomes]
rs698674	0.90[CEU][hapmap]
rs72977046	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72977051	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72977054	0.82[EUR][1000 genomes]
rs72977058	0.82[AMR][1000 genomes]
rs72977059	0.82[AMR][1000 genomes]
rs72977066	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72977068	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72977071	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72977074	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72977076	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72977077	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72977079	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72977082	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72977087	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72977090	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72977098	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72979010	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72979012	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72979014	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979024	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979026	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979027	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979028	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979029	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979030	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979031	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979033	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979035	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979037	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979040	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979042	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979043	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979047	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979050	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979054	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979056	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979058	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72979060	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979063	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979064	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979065	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979067	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979068	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979070	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979074	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979078	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979081	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979083	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72979085	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7612862	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7613608	0.82[EUR][1000 genomes]
rs7617576	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7618685	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7618942	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7619121	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7622801	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7622894	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7627814	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7628091	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7630367	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7630456	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7635537	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7640555	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7640640	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7645011	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7645261	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7645465	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757891	chr3:139925764-140524730	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv2759181	chr3:139925764-140524730	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv527831	chr3:139932966-140533823	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv34489	chr3:140009020-140469302	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv2757012	chr3:140009220-140460228	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv877546	chr3:140299603-140468370	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv997694	chr3:140324012-140464786	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1008123	chr3:140328825-140464786	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv460869	chr3:140330108-140450655	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv591864	chr3:140330108-140450655	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv818170	chr3:140330108-140454836	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv1008838	chr3:140355975-140588726	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv877547	chr3:140366948-140575287	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv829743	chr3:140384246-140559778	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv591865	chr3:140396022-140728850	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140443800-140445200	Enhancers	GM12878-XiMat	blood
2	chr3:140443800-140447000	Enhancers	HepG2	liver
3	chr3:140444000-140444800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:140444600-140447200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:140444600-140447400	Enhancers	ES-I3 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links