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	nsv888925	chr7:104047599-104170560	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	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	chr7:104052600-104053000	Bivalent Enhancer	Fetal Brain Male	brain
2	chr7:104052600-104053400	Enhancers	Brain Anterior Caudate	brain
3	chr7:104052800-104054200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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