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	nsv967016	chr3:50753594-50759813	Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50746600-50755400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:50750800-50755600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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