Variant report

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

rs_ID	r²[population]
rs28578707	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7014166	0.91[AFR][1000 genomes];1.00[AMR][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	nsv891045	chr8:77998659-78477561	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr8:78102400-78104400	Enhancers	GM12878-XiMat	blood

Quick Search:

Input of quick search could be: