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	nsv999046	chr3:70549472-70576944	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	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	chr3:70549800-70551800	Enhancers	Fetal Thymus	thymus
2	chr3:70550000-70551400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:70550400-70551200	Enhancers	Dnd41	blood

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