Variant report

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs73783729	0.90[AFR][1000 genomes]

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	nsv1015741	chr5:116525936-116665270	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116543000-116559000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:116557400-116558400	Weak transcription	Stomach Mucosa	stomach

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