Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10506433	1.00[YRI][hapmap]
rs11830499	1.00[ASN][1000 genomes]
rs11831039	1.00[ASN][1000 genomes]
rs11832185	1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs11834730	1.00[YRI][hapmap]
rs11836702	1.00[YRI][hapmap]
rs11836835	1.00[YRI][hapmap]
rs11837361	1.00[ASN][1000 genomes]
rs11837364	1.00[ASN][1000 genomes]
rs11837421	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11837618	1.00[YRI][hapmap]
rs12302719	1.00[ASN][1000 genomes]
rs17654807	1.00[YRI][hapmap]
rs17656359	1.00[YRI][hapmap]
rs17656662	1.00[YRI][hapmap]
rs17706308	1.00[YRI][hapmap]
rs17713184	1.00[YRI][hapmap]
rs3892748	1.00[YRI][hapmap]
rs73130983	1.00[ASN][1000 genomes]
rs7955714	1.00[ASN][1000 genomes]
rs7956690	1.00[ASN][1000 genomes]
rs7958639	1.00[ASN][1000 genomes]
rs7979256	1.00[ASN][1000 genomes]
rs7979621	1.00[ASN][1000 genomes]
rs9669548	1.00[YRI][hapmap]
rs9737799	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9739100	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039741	chr12:62046850-62491052	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv832435	chr12:62407000-62601835	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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