Variant report

rSNPs within LD-proxies of this variant (count:10)

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	esv1842873	chr4:20361842-20399168	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr4:20376200-20386600	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:20376600-20386000	Weak transcription	Fetal Lung	lung
3	chr4:20380200-20392600	Weak transcription	NHDF-Ad	bronchial

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