Variant report

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs10930261	1.00[CHB][hapmap]
rs11889300	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap]
rs11896680	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap]

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	nsv529384	chr2:167143465-167958752	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17614686	SLC38A11	cis	cerebellum	SCAN

Chromatin state (count:0 , 50 per page) page:

No data

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