Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11132858	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11931393	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12644221	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13114948	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs13145731	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1403211	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1533837	0.82[ASN][1000 genomes]
rs1568620	0.89[ASN][1000 genomes]
rs1568621	0.87[ASN][1000 genomes]
rs17662713	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1915996	0.89[ASN][1000 genomes]
rs1996831	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2331976	0.82[EUR][1000 genomes]
rs28702559	0.87[ASN][1000 genomes]
rs35465717	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6828494	0.81[EUR][1000 genomes]
rs6844817	0.82[EUR][1000 genomes]
rs7654851	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7680601	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9991006	0.82[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9995101	0.84[EUR][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	nsv596167	chr4:171576294-171672038	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv881141	chr4:171620514-171680223	Enhancers Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:171619800-171620600	Weak transcription	Aorta	Aorta
2	chr4:171620400-171621800	Enhancers	GM12878-XiMat	blood

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