Variant report

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10483756	0.90[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs11158452	0.89[JPT][hapmap]
rs12897538	0.90[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs2171876	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs36107257	0.83[EUR][1000 genomes]
rs7493979	0.81[CEU][hapmap];0.88[JPT][hapmap]
rs961066	0.82[CEU][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	nsv902015	chr14:63261862-63356253	Enhancers Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17834917	PRSS21	trans	lymphoblastoid	seeQTL

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

No data

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