Variant report

Variant	rs12761960
Chromosome Location	chr10:97507445-97507446
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs11592789	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11592809	0.89[CEU][hapmap]
rs11592937	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11593038	0.86[EUR][1000 genomes]
rs11594340	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11594687	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs11595122	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11595248	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs11596697	1.00[YRI][hapmap]
rs11598540	0.86[EUR][1000 genomes]
rs11599779	1.00[YRI][hapmap]
rs12763743	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs12765494	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12767650	0.89[CEU][hapmap];1.00[YRI][hapmap];0.89[EUR][1000 genomes]
rs12770313	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12770849	0.89[CEU][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes]
rs12774334	0.84[EUR][1000 genomes]
rs12775780	0.86[EUR][1000 genomes]
rs12779833	0.85[EUR][1000 genomes]
rs12780375	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs12782273	0.82[EUR][1000 genomes]
rs1409710	1.00[CEU][hapmap]
rs2275272	1.00[CEU][hapmap]
rs3176886	0.89[CEU][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs3176888	0.89[CEU][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes]
rs3181115	0.89[CEU][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34296389	0.85[EUR][1000 genomes]
rs34332904	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34460407	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs34630379	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34808745	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34832675	0.81[EUR][1000 genomes]
rs34833309	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34836127	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35051706	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35691144	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35700869	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35712039	0.81[EUR][1000 genomes]
rs35822210	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs35987262	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3793751	1.00[CEU][hapmap]
rs57670810	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs66751616	0.82[EUR][1000 genomes]
rs67783179	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs67857430	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs68078796	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs71482367	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs71482374	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs71482376	0.87[EUR][1000 genomes]
rs71482377	0.87[EUR][1000 genomes]
rs71482378	0.88[EUR][1000 genomes]

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	nsv526180	chr10:97332195-97511037	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv531923	chr10:97366055-97725757	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97505800-97508200	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr10:97506600-97509200	Weak transcription	Primary B cells from peripheral blood	blood
3	chr10:97507000-97507600	Strong transcription	Primary B cells from cord blood	blood

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