Variant report

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs8022920	1.00[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	nsv1047924	chr14:85826280-85868228	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85830200-85831600	Weak transcription	Fetal Lung	lung
2	chr14:85830600-85831600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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