Variant report

rSNPs within LD-proxies of this variant (count:5)

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	nsv1042953	chr14:63314591-63384260	Enhancers Weak transcription	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	chr14:63380600-63381600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr14:63381400-63381800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr14:63381400-63382000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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