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	esv3325685	chr14:84564549-84564980	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

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Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84558600-84566400	Weak transcription	Fetal Stomach	stomach
2	chr14:84564400-84564800	Enhancers	Stomach Mucosa	stomach

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