Variant report

rSNPs within LD-proxies of this variant (count:7)

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	nsv565376	chr14:84612088-84644822	Enhancers Weak transcription	TF binding region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84618600-84618800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr14:84618600-84618800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:84618600-84619200	Enhancers	Spleen	Spleen

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