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	nsv1036417	chr9:103478028-103509840	Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	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	chr9:103477800-103478200	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr9:103477800-103478200	Enhancers	Fetal Brain Male	brain
3	chr9:103478000-103481000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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