Variant report

Variant	rs7656709
Chromosome Location	chr4:85994452-85994453
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10002152	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10002878	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11097034	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11097036	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11734281	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11937574	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13120826	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13120830	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13126594	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17009477	0.93[EUR][1000 genomes]
rs17009479	0.93[EUR][1000 genomes]
rs17009666	1.00[CEU][hapmap]
rs2869271	0.93[EUR][1000 genomes]
rs4235069	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4235074	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4235075	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4283651	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4295250	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4314278	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4315777	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4321625	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4321626	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4342179	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4348084	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4374618	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4374619	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4398517	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4455405	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4495030	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4507353	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4527465	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4543102	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4554065	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4558866	1.00[CEU][hapmap]
rs4597823	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4613556	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4693111	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4693112	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4693113	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs55696529	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56078987	0.93[EUR][1000 genomes]
rs56276119	0.93[EUR][1000 genomes]
rs56689597	0.93[EUR][1000 genomes]
rs56793437	0.93[EUR][1000 genomes]
rs56999015	0.93[EUR][1000 genomes]
rs57443529	0.93[EUR][1000 genomes]
rs57625945	0.93[EUR][1000 genomes]
rs57668646	0.89[EUR][1000 genomes]
rs58339031	0.93[EUR][1000 genomes]
rs58395301	0.82[EUR][1000 genomes]
rs59106945	0.93[EUR][1000 genomes]
rs59475008	0.93[EUR][1000 genomes]
rs59638292	0.93[EUR][1000 genomes]
rs61447165	0.93[EUR][1000 genomes]
rs72962210	0.93[EUR][1000 genomes]
rs7655309	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7662243	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7674965	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7689296	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7694774	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9685046	1.00[CEU][hapmap]
rs9884829	0.93[AMR][1000 genomes];0.90[EUR][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	esv1829655	chr4:85577491-86292692	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv519588	chr4:85762385-86591202	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	esv3367963	chr4:85911017-86246036	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv461566	chr4:85988032-86725502	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
5	nsv594747	chr4:85988032-86725502	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
6	nsv967670	chr4:85989733-85994729	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85993600-85995000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:85994000-85994800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:85994400-85995000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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