Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11613585	1.00[JPT][hapmap]
rs11615631	1.00[JPT][hapmap]
rs12299018	1.00[YRI][hapmap]
rs12312776	1.00[ASN][1000 genomes]
rs12318722	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12318972	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17033429	1.00[ASN][1000 genomes]
rs17033447	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73183655	1.00[ASN][1000 genomes]
rs73183658	1.00[ASN][1000 genomes]
rs73183659	1.00[ASN][1000 genomes]
rs73183660	1.00[ASN][1000 genomes]
rs73183661	1.00[ASN][1000 genomes]
rs73183663	1.00[ASN][1000 genomes]
rs73183668	1.00[ASN][1000 genomes]
rs73183672	1.00[ASN][1000 genomes]
rs73183673	1.00[ASN][1000 genomes]
rs73183674	1.00[ASN][1000 genomes]
rs73183675	1.00[ASN][1000 genomes]
rs73183676	1.00[ASN][1000 genomes]

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	nsv832501	chr12:103463927-103648825	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	esv1824379	chr12:103501562-103549931	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	9 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	chr12:103521800-103524800	Enhancers	Liver	Liver
2	chr12:103523000-103524000	Enhancers	Fetal Intestine Small	intestine

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