Variant report

Variant	rs11234262
Chromosome Location	chr11:84712484-84712485
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10792795	0.95[CEU][hapmap];0.89[CHB][hapmap];0.90[JPT][hapmap];0.96[YRI][hapmap]
rs10792796	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10898338	0.95[CHB][hapmap]
rs10898339	0.95[CHB][hapmap]
rs10898341	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[YRI][hapmap]
rs11234253	0.95[CHB][hapmap]
rs11234256	0.82[EUR][1000 genomes]
rs11234263	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11234269	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1470843	0.80[ASN][1000 genomes]
rs17741917	0.95[CHB][hapmap]
rs1940130	0.80[ASN][1000 genomes]
rs2374578	1.00[CEU][hapmap];0.84[CHB][hapmap]
rs2374579	0.80[CEU][hapmap]
rs2444253	0.87[YRI][hapmap]
rs2508322	0.93[YRI][hapmap]
rs34813295	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs349057	0.83[CEU][hapmap];0.81[AMR][1000 genomes]
rs349060	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs349063	0.90[YRI][hapmap]
rs349068	0.85[YRI][hapmap]
rs349069	0.89[CHB][hapmap];0.89[YRI][hapmap]
rs349076	0.87[CEU][hapmap]
rs349078	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs349080	0.96[CEU][hapmap];0.84[CHB][hapmap];0.86[JPT][hapmap];0.83[YRI][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs349082	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs349083	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs349084	1.00[CEU][hapmap];0.80[CHB][hapmap];0.82[YRI][hapmap]
rs349085	0.87[CEU][hapmap]
rs349086	0.96[CEU][hapmap]
rs349088	0.82[YRI][hapmap]
rs349089	0.96[CEU][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35728575	0.83[ASN][1000 genomes]
rs3844142	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3851172	0.95[CHB][hapmap];0.80[ASN][1000 genomes]
rs3851173	1.00[CEU][hapmap];0.95[CHB][hapmap];0.81[EUR][1000 genomes]
rs3851174	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[YRI][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3862780	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3862781	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3907015	0.95[CEU][hapmap];0.84[CHB][hapmap];0.90[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3911270	0.95[CHB][hapmap];0.82[ASN][1000 genomes]
rs3911271	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3911273	1.00[CEU][hapmap];0.95[CHB][hapmap]
rs3933734	0.89[CHB][hapmap];0.90[YRI][hapmap]
rs4121472	0.90[CHB][hapmap];0.87[YRI][hapmap]
rs4121473	0.90[CHB][hapmap];0.96[YRI][hapmap]
rs4271408	0.84[CHB][hapmap];0.83[YRI][hapmap]
rs4943908	1.00[CEU][hapmap];0.95[CHB][hapmap]
rs506422	0.86[YRI][hapmap]
rs550970	0.84[CHB][hapmap];0.93[YRI][hapmap]
rs573767	0.89[YRI][hapmap]
rs582399	0.80[ASN][1000 genomes]
rs613972	1.00[CEU][hapmap];0.81[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs616320	0.96[CEU][hapmap];0.81[JPT][hapmap];0.87[YRI][hapmap];0.82[AMR][1000 genomes]
rs619848	1.00[CEU][hapmap];0.81[YRI][hapmap]
rs630015	0.96[CEU][hapmap]
rs634050	0.84[CHB][hapmap];0.95[JPT][hapmap];0.89[YRI][hapmap];0.84[ASN][1000 genomes]
rs635860	0.89[YRI][hapmap]
rs652852	0.84[CHB][hapmap];0.89[YRI][hapmap]
rs653885	0.90[YRI][hapmap]
rs6592218	1.00[CEU][hapmap]
rs6592219	1.00[CEU][hapmap];0.80[CHB][hapmap]
rs6592223	0.81[CHB][hapmap];0.82[JPT][hapmap];0.93[YRI][hapmap]
rs6592225	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs6592228	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6592229	0.96[CEU][hapmap];0.97[YRI][hapmap]
rs7105774	0.95[CEU][hapmap];0.89[CHB][hapmap];0.86[JPT][hapmap];0.89[YRI][hapmap]
rs7111336	0.96[CEU][hapmap];0.93[YRI][hapmap]
rs7112064	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7125600	1.00[CEU][hapmap];0.90[CHB][hapmap];0.96[YRI][hapmap]
rs7127826	0.95[CHB][hapmap];0.90[YRI][hapmap]
rs7131501	0.95[CEU][hapmap];0.85[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7131533	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7482922	1.00[CHB][hapmap];0.96[YRI][hapmap]
rs7925898	0.90[CHB][hapmap];0.86[YRI][hapmap]
rs7929647	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs7931733	0.96[CEU][hapmap];0.87[JPT][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7933636	0.81[JPT][hapmap];0.80[YRI][hapmap]
rs7943194	0.95[CHB][hapmap]
rs7949547	0.89[CHB][hapmap];0.90[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948410	chr11:83918339-84812001	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1048051	chr11:84419442-84784233	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv541109	chr11:84419442-84784233	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv898041	chr11:84642163-84722252	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv430415	chr11:84661652-84833852	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1055097	chr11:84672444-84810441	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1040393	chr11:84708402-84866594	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	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	chr11:84711400-84714800	Weak transcription	Aorta	Aorta

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