Variant report

rSNPs within LD-proxies of this variant (count:6)

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	nsv870459	chr1:102112168-102166616	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:102162800-102164600	Weak transcription	Fetal Brain Male	brain
2	chr1:102163200-102165000	Weak transcription	Fetal Heart	heart
3	chr1:102163600-102166400	Weak transcription	Dnd41	blood

Quick Search:

Input of quick search could be: