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	nsv984341	chr16:64770082-64771386	Weak transcription Enhancers	TF binding region lncRNA	2 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	chr16:64767600-64772200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr16:64771200-64772400	Weak transcription	Osteobl	bone

Quick Search:

Input of quick search could be: