Variant report

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

rs_ID	r²[population]
rs10153880	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1025831	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1025832	0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12470261	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12478109	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13393611	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1837778	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs36050170	0.91[ASN][1000 genomes]
rs474275	0.91[ASN][1000 genomes]
rs475172	0.91[ASN][1000 genomes]
rs488610	0.93[ASN][1000 genomes]
rs4954843	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4954844	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs521254	0.92[ASN][1000 genomes]
rs538308	0.91[ASN][1000 genomes]
rs540441	0.93[ASN][1000 genomes]
rs540949	0.91[ASN][1000 genomes]
rs567499	0.91[ASN][1000 genomes]
rs62171950	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6747606	0.91[ASN][1000 genomes]
rs9646668	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][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	nsv583193	chr2:141365171-141415043	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141384400-141385200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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