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	esv3346101	chr11:105819810-105820164	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	chr11:105818800-105826600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr11:105819400-105820600	Enhancers	Hela-S3	cervix

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