Variant report

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs7724723	1.00[AFR][1000 genomes]
rs7727204	1.00[AFR][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	nsv830287	chr5:50380059-50509674	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 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	chr5:50495600-50497000	Enhancers	Fetal Brain Female	brain

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