Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1457761	0.91[CHB][hapmap]
rs163301	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs163303	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs163304	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs181949	0.81[CEU][hapmap];0.82[CHB][hapmap]
rs337685	0.82[CHB][hapmap]
rs337689	0.91[CHB][hapmap]
rs337691	0.82[CHB][hapmap]
rs337699	0.91[CHB][hapmap]
rs36938	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs36942	0.96[CEU][hapmap];0.82[CHB][hapmap];0.85[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs36945	0.88[CEU][hapmap];0.82[CHB][hapmap];0.85[JPT][hapmap]
rs36946	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs36947	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs36949	0.81[CEU][hapmap];0.82[CHB][hapmap]
rs36950	0.81[CEU][hapmap];0.82[CHB][hapmap]
rs36955	0.82[AMR][1000 genomes]
rs36959	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs388084	0.91[CHB][hapmap]
rs636200	0.87[AMR][1000 genomes];0.95[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	nsv882728	chr5:113651694-113731423	Bivalent/Poised TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr5:113664600-113666600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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