Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10081237	1.00[ASW][hapmap];1.00[AMR][1000 genomes]
rs10225020	1.00[YRI][hapmap]
rs10239617	1.00[AMR][1000 genomes]
rs10240626	1.00[AMR][1000 genomes]
rs10252488	1.00[AMR][1000 genomes]
rs10254174	1.00[ASW][hapmap];1.00[AMR][1000 genomes]
rs10262861	1.00[AMR][1000 genomes]
rs17865220	1.00[YRI][hapmap]
rs17865523	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17865864	1.00[YRI][hapmap]
rs17866100	1.00[YRI][hapmap]
rs17866102	1.00[YRI][hapmap]
rs17866212	1.00[YRI][hapmap]
rs17866398	1.00[YRI][hapmap]
rs17866773	1.00[YRI][hapmap]
rs17866950	1.00[YRI][hapmap]
rs17867019	1.00[YRI][hapmap]
rs17867043	1.00[AMR][1000 genomes]
rs17867257	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17869369	1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17869370	1.00[AMR][1000 genomes]
rs17869597	1.00[YRI][hapmap]
rs17875084	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831121	chr7:126593363-126774413	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv889189	chr7:126699088-126963028	Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No data

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