Variant report

Variant overlapped rSNPs/rCNVs (count:2 , 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
2	esv1690560	chr14:84578320-84578322	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

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

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