Variant report

Variant	rs55696529
Chromosome Location	chr4:86039180-86039181
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10002152	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10002878	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11097034	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11097036	0.86[AMR][1000 genomes]
rs11734281	0.86[AMR][1000 genomes]
rs11937574	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13120826	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs17009477	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17009479	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2869271	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4235069	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4235074	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4235075	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4283651	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4295250	0.83[AMR][1000 genomes]
rs4314278	0.83[AMR][1000 genomes]
rs4315777	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4321625	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4321626	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4342179	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4348084	0.83[AMR][1000 genomes]
rs4398517	0.83[AMR][1000 genomes]
rs4455405	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4507353	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4527465	0.83[AMR][1000 genomes]
rs4554065	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4613556	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4693112	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4693113	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs56078987	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56276119	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56689597	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56793437	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56999015	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57443529	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57625945	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57668646	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58339031	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs58395301	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs59106945	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59475008	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59638292	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61447165	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72962210	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7655309	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7656709	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7662243	0.83[AMR][1000 genomes]
rs7674965	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7694774	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9884829	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	nsv470048	chr4:85998783-86720838	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
7	nsv427685	chr4:86032872-86340548	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86038800-86039600	Enhancers	Adipose Nuclei	Adipose
2	chr4:86039000-86039200	Enhancers	Pancreas	Pancrea

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