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	nsv518279	chr14:84598224-84612088	Enhancers Active TSS	n/a	n/a	inside rSNPs	diseases

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Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84610200-84611400	Enhancers	HUVEC	blood vessel
2	chr14:84610200-84612000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr14:84610600-84612000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr14:84610800-84611600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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