Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs11079562	0.89[EUR][1000 genomes]
rs11867807	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11871337	0.90[EUR][1000 genomes]
rs12150224	0.82[EUR][1000 genomes]
rs2067622	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28410529	0.87[AFR][1000 genomes]
rs57733055	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57840776	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59371945	0.90[EUR][1000 genomes]
rs7209620	0.86[EUR][1000 genomes]
rs7211594	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7225073	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72845340	0.90[EUR][1000 genomes]
rs72845343	0.89[EUR][1000 genomes]
rs72845363	0.94[EUR][1000 genomes]
rs72845368	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72853506	0.99[EUR][1000 genomes]
rs8067645	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8072284	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs929515	0.82[AFR][1000 genomes]
rs9896135	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9903141	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9903508	0.82[AFR][1000 genomes]
rs9909786	0.97[EUR][1000 genomes]
rs9910848	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9911786	0.86[EUR][1000 genomes]

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	nsv482610	chr17:63214370-63372334	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 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	chr17:63290800-63300200	Weak transcription	Fetal Lung	lung
2	chr17:63290800-63301200	Weak transcription	Pancreas	Pancrea

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