Variant report

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

rs_ID	r²[population]
rs17092201	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7930222	0.85[AMR][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	nsv556230	chr11:106676942-106704250	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106700400-106705200	Weak transcription	Fetal Heart	heart

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