Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10506261	1.00[JPT][hapmap]
rs10506262	1.00[JPT][hapmap]
rs10748423	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10880780	1.00[JPT][hapmap]
rs11183000	1.00[JPT][hapmap]
rs11183004	1.00[JPT][hapmap]
rs11183009	1.00[JPT][hapmap]
rs11183028	1.00[JPT][hapmap]
rs11183040	1.00[JPT][hapmap]
rs11612531	1.00[JPT][hapmap]
rs12230667	1.00[JPT][hapmap]
rs12314896	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs12578593	0.94[JPT][hapmap]
rs12809717	1.00[JPT][hapmap]
rs12821880	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12829496	1.00[JPT][hapmap]
rs1986426	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2408260	1.00[JPT][hapmap]
rs2408315	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2408316	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs36030426	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4469956	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4768611	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6582546	1.00[JPT][hapmap]
rs7302256	1.00[JPT][hapmap]
rs7307549	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs7307697	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7965912	1.00[JPT][hapmap]
rs9788251	1.00[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832395	chr12:45841765-46039297	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr12:45827600-45842800	Weak transcription	Aorta	Aorta

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