Variant report

rSNPs within LD-proxies of this variant (count:10)

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

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104082800-104084000	Enhancers	Fetal Brain Female	brain
2	chr7:104083200-104084800	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr7:104083600-104084400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

Quick Search: