Variant report

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12065426	0.83[ASN][1000 genomes]
rs12077271	0.83[ASN][1000 genomes]
rs12080769	0.83[ASN][1000 genomes]
rs12565753	0.83[ASN][1000 genomes]
rs12745058	0.83[ASN][1000 genomes]
rs34025182	0.83[ASN][1000 genomes]
rs34332254	0.83[ASN][1000 genomes]
rs34931189	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35379498	0.83[ASN][1000 genomes]
rs35607505	0.83[ASN][1000 genomes]
rs57032935	0.82[ASN][1000 genomes]
rs61828886	0.85[ASN][1000 genomes]
rs61828887	0.86[ASN][1000 genomes]
rs61828888	0.86[ASN][1000 genomes]
rs6696443	0.83[ASN][1000 genomes]
rs72637251	0.90[AMR][1000 genomes]
rs7413754	0.83[ASN][1000 genomes]
rs7516544	0.83[ASN][1000 genomes]
rs7521536	0.83[ASN][1000 genomes]
rs7524403	0.83[ASN][1000 genomes]
rs7524592	0.83[ASN][1000 genomes]
rs7525100	0.82[ASN][1000 genomes]
rs7529089	0.83[ASN][1000 genomes]
rs7529377	0.83[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	nsv872549	chr1:173509586-173546835	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:173527400-173530600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:173528600-173530200	Enhancers	Adipose Nuclei	Adipose
3	chr1:173529400-173529600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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