Variant report

Variant	rs11229692
Chromosome Location	chr11:58680127-58680128
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 104 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs10459028	0.93[EUR][1000 genomes]
rs10792206	0.83[ASN][1000 genomes]
rs10792207	0.84[ASN][1000 genomes]
rs10896872	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10896873	0.84[ASN][1000 genomes]
rs10896874	0.84[ASN][1000 genomes]
rs10896875	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10896876	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs10896877	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10896878	0.84[ASN][1000 genomes]
rs10896879	0.84[ASN][1000 genomes]
rs10896880	0.84[ASN][1000 genomes]
rs10896882	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10896883	0.82[ASN][1000 genomes]
rs10896884	0.82[ASN][1000 genomes]
rs11229687	0.83[ASN][1000 genomes]
rs11229688	0.84[ASN][1000 genomes]
rs11229689	0.84[ASN][1000 genomes]
rs11229693	0.84[ASN][1000 genomes]
rs11229694	0.84[ASN][1000 genomes]
rs11229695	0.84[ASN][1000 genomes]
rs11229701	0.84[ASN][1000 genomes]
rs11229704	0.84[ASN][1000 genomes]
rs11229705	0.84[ASN][1000 genomes]
rs11229711	0.82[ASN][1000 genomes]
rs11229717	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11229721	0.93[EUR][1000 genomes]
rs11229722	0.93[EUR][1000 genomes]
rs11229723	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes]
rs11229731	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11229742	0.93[EUR][1000 genomes]
rs11229746	0.93[EUR][1000 genomes]
rs11229747	0.86[EUR][1000 genomes]
rs11229748	0.86[EUR][1000 genomes]
rs11229749	0.93[EUR][1000 genomes]
rs11229755	0.93[EUR][1000 genomes]
rs11229762	0.93[EUR][1000 genomes]
rs11229766	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes]
rs11229767	0.93[EUR][1000 genomes]
rs11229774	0.93[EUR][1000 genomes]
rs11229775	0.93[EUR][1000 genomes]
rs11229779	0.85[EUR][1000 genomes]
rs11229787	0.93[EUR][1000 genomes]
rs11229791	0.93[EUR][1000 genomes]
rs11229802	0.93[EUR][1000 genomes]
rs11494143	0.93[EUR][1000 genomes]
rs11537230	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11560958	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12049866	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12222588	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12222597	0.84[ASN][1000 genomes]
rs12223443	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12226515	0.93[EUR][1000 genomes]
rs12277628	0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs12278662	0.84[ASN][1000 genomes]
rs12281983	0.83[ASN][1000 genomes]
rs12292314	0.84[ASN][1000 genomes]
rs17153331	0.93[EUR][1000 genomes]
rs1808064	0.84[ASN][1000 genomes]
rs1815856	0.87[JPT][hapmap]
rs1893627	0.84[ASN][1000 genomes]
rs1893628	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs1893629	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs1938786	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs1943264	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2156344	0.84[ASN][1000 genomes]
rs2156345	0.84[ASN][1000 genomes]
rs2156349	0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs35613819	0.93[EUR][1000 genomes]
rs3740949	0.93[EUR][1000 genomes]
rs3740950	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3740952	0.93[EUR][1000 genomes]
rs4271397	0.82[ASN][1000 genomes]
rs4547111	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4573693	0.84[ASN][1000 genomes]
rs4616060	0.93[EUR][1000 genomes]
rs4939243	0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs56155456	0.84[ASN][1000 genomes]
rs58848038	0.82[ASN][1000 genomes]
rs61889804	0.84[ASN][1000 genomes]
rs61889805	0.84[ASN][1000 genomes]
rs61892604	0.83[ASN][1000 genomes]
rs7108461	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs7114348	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7118637	0.83[JPT][hapmap]
rs7126489	0.93[JPT][hapmap];0.84[ASN][1000 genomes]
rs7129011	0.83[JPT][hapmap];0.83[ASN][1000 genomes]
rs7129475	0.93[EUR][1000 genomes]
rs7930111	0.84[ASN][1000 genomes]
rs7939049	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7947356	0.85[EUR][1000 genomes]
rs7947971	0.93[EUR][1000 genomes]
rs948819	0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs9787921	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050013	chr11:58394598-59221090	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv948365	chr11:58515163-59156405	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
3	esv3444895	chr11:58614102-58779384	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	esv3445007	chr11:58638330-58709867	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	esv3502182	chr11:58668199-58731237	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv3502181	chr11:58668236-58731215	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	esv3478019	chr11:58668282-58731214	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	esv3478030	chr11:58668282-58731214	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	esv3502183	chr11:58668353-58731177	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	esv3393019	chr11:58679419-58880845	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58673800-58682200	Weak transcription	NH-A	brain
2	chr11:58674000-58682200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:58674200-58682200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr11:58679200-58680200	Enhancers	NHEK	skin
5	chr11:58679800-58682200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr11:58680000-58682000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:58680000-58682000	Weak transcription	HMEC	breast
8	chr11:58680000-58682200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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