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	esv3364092	chr14:84577449-84579347	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84577400-84579600	Enhancers	Stomach Mucosa	stomach
2	chr14:84578600-84579800	Enhancers	HUVEC	blood vessel

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