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	esv1792427	chr5:135744555-135755386	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:135742200-135754400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:135745000-135745800	Enhancers	HUVEC	blood vessel

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