Variant report

rSNPs within LD-proxies of this variant (count:4)

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	nsv1009857	chr3:68696340-68746434	Enhancers Weak transcription	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	chr3:68711000-68715600	Weak transcription	Aorta	Aorta
2	chr3:68711400-68713000	Weak transcription	Colon Smooth Muscle	Colon
3	chr3:68712000-68715400	Weak transcription	Stomach Smooth Muscle	stomach

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