Variant report

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	nsv1028244	chr4:160370159-160395135	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

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Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160368200-160372400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:160368200-160376600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr4:160368400-160390200	Weak transcription	NHEK	skin

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