Variant report

Variant	rs4061832
Chromosome Location	chr3:98053033-98053034
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1008191	0.86[ASN][1000 genomes]
rs1123188	0.85[ASN][1000 genomes]
rs11929098	0.89[ASN][1000 genomes]
rs12631405	0.83[ASN][1000 genomes]
rs12632368	0.86[ASN][1000 genomes]
rs12632378	0.87[ASN][1000 genomes]
rs12636942	0.89[ASN][1000 genomes]
rs12637340	0.86[CHB][hapmap]
rs12637769	0.85[ASN][1000 genomes]
rs12638749	0.89[ASN][1000 genomes]
rs12639159	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13063426	0.82[ASN][1000 genomes]
rs13066249	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13067773	0.89[ASN][1000 genomes]
rs13075581	0.85[ASN][1000 genomes]
rs13079269	0.89[ASN][1000 genomes]
rs13080412	0.89[ASN][1000 genomes]
rs13086001	0.89[ASN][1000 genomes]
rs13088051	0.86[ASN][1000 genomes]
rs13096400	0.89[ASN][1000 genomes]
rs1391156	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1497531	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1497532	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16839427	0.81[MEX][hapmap]
rs16839647	0.89[ASN][1000 genomes]
rs1846081	0.82[ASN][1000 genomes]
rs1964019	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1964021	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2132898	0.89[ASN][1000 genomes]
rs2316269	0.89[ASN][1000 genomes]
rs34156823	0.83[ASN][1000 genomes]
rs34721537	0.89[ASN][1000 genomes]
rs34829706	0.89[ASN][1000 genomes]
rs35015849	0.89[ASN][1000 genomes]
rs35133117	0.89[ASN][1000 genomes]
rs35370148	0.89[ASN][1000 genomes]
rs35468350	0.89[ASN][1000 genomes]
rs35584221	0.85[ASN][1000 genomes]
rs35627913	0.83[ASN][1000 genomes]
rs35807053	0.88[ASN][1000 genomes]
rs36064521	0.86[ASN][1000 genomes]
rs3937916	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4241472	0.86[CHB][hapmap]
rs4388016	0.86[AMR][1000 genomes]
rs4519740	0.89[ASN][1000 genomes]
rs4603997	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4857363	0.86[ASN][1000 genomes]
rs56220142	0.89[ASN][1000 genomes]
rs57420324	0.83[AMR][1000 genomes]
rs62267258	0.83[ASN][1000 genomes]
rs6805802	0.89[ASN][1000 genomes]
rs71311371	0.88[ASN][1000 genomes]
rs73854481	0.83[ASN][1000 genomes]
rs7613182	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7641621	0.89[ASN][1000 genomes]
rs7641820	0.89[ASN][1000 genomes]
rs924227	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9790053	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004820	chr3:97852875-98169488	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1000834	chr3:97859880-98095473	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	esv1842860	chr3:97934241-98075543	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1009918	chr3:97946030-98155450	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr3:98053000-98053400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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