Variant report

Variant	rs7776617
Chromosome Location	chr7:121065112-121065113
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:121033106..121035000-chr7:121064896..121066806,2	K562	blood:
2	chr7:121063601..121065601-chr7:121068374..121070365,2	MCF-7	breast:
3	chr7:121060143..121062548-chr7:121064145..121066050,2	MCF-7	breast:
4	chr7:121059489..121061007-chr7:121064201..121066957,2	K562	blood:

Extended variants
information (count: 122 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs10215001	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10215613	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10215690	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10215696	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10224285	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10224531	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10229623	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10240942	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10255192	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10259018	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10264556	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10267770	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10270768	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11520945	0.84[EUR][1000 genomes]
rs11521035	0.83[EUR][1000 genomes]
rs11521036	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11971157	0.91[AFR][1000 genomes]
rs11972392	0.97[YRI][hapmap];0.92[AFR][1000 genomes]
rs11982913	0.90[AFR][1000 genomes]
rs12532811	0.91[AFR][1000 genomes]
rs12536097	0.86[AFR][1000 genomes]
rs12706345	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12706347	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12706348	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12706349	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13233332	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13237689	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13237707	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13237717	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13242463	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1406191	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1534519	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1534520	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1534521	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1534522	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1609291	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1881373	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2049703	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2141357	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2141359	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2178187	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2244845	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2244847	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2244849	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2263404	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2402564	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2402565	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2402566	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2402567	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2463645	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2463646	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2697168	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2697171	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2697172	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2697173	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2697174	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2697188	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2697189	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2697190	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2707484	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2707485	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2707490	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2707502	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28609751	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28623616	0.81[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs2950813	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2952571	0.92[ASN][1000 genomes]
rs2952573	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2952575	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2952577	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4507708	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4541839	0.81[EUR][1000 genomes]
rs4593469	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4731012	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4731013	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4731014	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4731015	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56055102	0.85[AFR][1000 genomes]
rs56403550	0.90[EUR][1000 genomes]
rs56669615	0.91[AFR][1000 genomes]
rs57826126	0.90[AFR][1000 genomes]
rs62475037	0.90[EUR][1000 genomes]
rs62475038	0.90[EUR][1000 genomes]
rs62475039	0.90[EUR][1000 genomes]
rs62475040	0.90[EUR][1000 genomes]
rs62476180	0.90[EUR][1000 genomes]
rs62476184	0.90[EUR][1000 genomes]
rs62476187	0.88[EUR][1000 genomes]
rs62476208	0.85[EUR][1000 genomes]
rs62476209	0.82[EUR][1000 genomes]
rs62476210	0.83[EUR][1000 genomes]
rs62476211	0.81[EUR][1000 genomes]
rs6466783	0.88[AFR][1000 genomes]
rs6466785	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs67085750	0.91[AFR][1000 genomes]
rs67303703	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6950058	0.96[YRI][hapmap];0.91[AFR][1000 genomes]
rs6954718	0.96[YRI][hapmap];0.91[AFR][1000 genomes]
rs6961822	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6962156	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73442206	0.91[AFR][1000 genomes]
rs7782605	0.92[AFR][1000 genomes]
rs7794700	0.90[EUR][1000 genomes]
rs7795121	0.90[EUR][1000 genomes]
rs7809856	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7809875	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9641666	0.85[EUR][1000 genomes]
rs9656282	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9656283	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9656284	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9656285	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9886342	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9942703	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025430	chr7:120638930-121179289	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1026322	chr7:120841937-121188037	Weak transcription Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv539102	chr7:120841937-121188037	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	esv2755350	chr7:120848049-121119049	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv1032054	chr7:120926379-121432971	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv539103	chr7:120926379-121432971	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
7	nsv428507	chr7:121037303-121191934	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	esv2757238	chr7:121059871-121089955	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	esv2759559	chr7:121059871-121089955	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121056800-121065800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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