Variant report

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17145044	0.83[EUR][1000 genomes]
rs17145080	0.83[EUR][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	nsv5655	chr7:21728469-21773203	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	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	chr7:21731600-21732600	Enhancers	Brain Germinal Matrix	brain
2	chr7:21732200-21733000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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