Variant report

Variant	rs10750883
Chromosome Location	chr11:57872058-57872059
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10750878	0.88[CEU][hapmap];0.82[CHB][hapmap];0.83[JPT][hapmap]
rs10750880	0.84[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10750881	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10750882	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs10792133	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10792135	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs10896696	0.89[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs10896705	0.83[JPT][hapmap]
rs11229247	0.94[CEU][hapmap];0.95[CHB][hapmap];0.96[JPT][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11229250	0.94[CEU][hapmap];0.95[CHB][hapmap];0.96[JPT][hapmap]
rs1123307	0.89[CEU][hapmap];0.81[CHB][hapmap];0.92[EUR][1000 genomes]
rs12226617	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12363350	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1447169	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs1451326	0.82[CHB][hapmap];0.83[JPT][hapmap];0.89[YRI][hapmap]
rs1868043	0.89[CEU][hapmap];0.80[CHB][hapmap]
rs2003375	0.89[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs2167358	0.89[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs3853677	1.00[JPT][hapmap]
rs3974323	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs4939176	0.88[CEU][hapmap];0.82[CHB][hapmap];0.83[JPT][hapmap];0.92[EUR][1000 genomes]
rs4939182	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs6591455	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7109726	0.94[CEU][hapmap];0.95[CHB][hapmap];0.96[JPT][hapmap]
rs7110748	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs7117711	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7118536	0.88[CEU][hapmap];0.82[CHB][hapmap];0.83[JPT][hapmap]
rs716945	0.87[JPT][hapmap]
rs921133	0.82[CEU][hapmap];0.83[JPT][hapmap]
rs976429	0.89[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes]
rs976430	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044030	chr11:57073395-58035564	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
2	nsv541047	chr11:57073395-58035564	Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
3	nsv1054205	chr11:57544264-58358509	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
4	nsv897589	chr11:57623815-58052357	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv832165	chr11:57806024-58009076	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
6	nsv832166	chr11:57852031-58006189	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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