Variant report

Variant	rs58124926
Chromosome Location	chr11:107702002-107702003
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:107701670..107703248-chr11:107728191..107729812,2	MCF-7	breast:
2	chr11:107693861..107695588-chr11:107701609..107703172,2	K562	blood:

Variant related genes	Relation type
ENSG00000110660	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10890764	0.95[EUR][1000 genomes]
rs11212379	0.82[EUR][1000 genomes]
rs11212383	0.87[EUR][1000 genomes]
rs11212389	0.95[EUR][1000 genomes]
rs11212390	0.95[EUR][1000 genomes]
rs11212391	0.95[EUR][1000 genomes]
rs11212392	0.95[EUR][1000 genomes]
rs11212393	0.95[EUR][1000 genomes]
rs11212394	0.95[EUR][1000 genomes]
rs11212395	0.95[EUR][1000 genomes]
rs11212396	0.95[EUR][1000 genomes]
rs11212397	0.95[EUR][1000 genomes]
rs11212398	0.95[EUR][1000 genomes]
rs11212400	0.95[EUR][1000 genomes]
rs12098896	0.95[EUR][1000 genomes]
rs12099368	0.95[EUR][1000 genomes]
rs12146456	0.95[EUR][1000 genomes]
rs12146459	0.95[EUR][1000 genomes]
rs12270982	0.87[EUR][1000 genomes]
rs12271120	0.95[EUR][1000 genomes]
rs12278904	0.95[EUR][1000 genomes]
rs12279264	0.91[EUR][1000 genomes]
rs12281160	0.95[EUR][1000 genomes]
rs12282500	1.00[ASN][1000 genomes]
rs12288093	0.95[EUR][1000 genomes]
rs12289394	0.97[ASN][1000 genomes]
rs12291200	0.95[EUR][1000 genomes]
rs12292050	0.95[EUR][1000 genomes]
rs12292254	0.95[EUR][1000 genomes]
rs12293650	0.95[EUR][1000 genomes]
rs503151	1.00[ASN][1000 genomes]
rs57429831	0.95[EUR][1000 genomes]
rs58472728	1.00[ASN][1000 genomes]
rs59036211	0.95[EUR][1000 genomes]
rs60539601	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66625589	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs67596776	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7118580	0.95[EUR][1000 genomes]
rs7120382	0.82[EUR][1000 genomes]
rs72999546	0.82[EUR][1000 genomes]
rs73001540	0.95[EUR][1000 genomes]
rs73001547	0.95[EUR][1000 genomes]
rs73001550	0.95[EUR][1000 genomes]
rs73001554	0.95[EUR][1000 genomes]
rs73001562	0.95[EUR][1000 genomes]
rs73001563	0.95[EUR][1000 genomes]
rs73001566	0.95[EUR][1000 genomes]
rs73003327	0.95[EUR][1000 genomes]
rs73003344	0.95[EUR][1000 genomes]
rs73003346	0.95[EUR][1000 genomes]
rs73003355	0.95[EUR][1000 genomes]
rs73003360	0.95[EUR][1000 genomes]
rs73003382	0.95[EUR][1000 genomes]
rs73003384	0.95[EUR][1000 genomes]
rs73005370	0.91[EUR][1000 genomes]
rs73546814	0.93[ASN][1000 genomes]
rs73546826	1.00[ASN][1000 genomes]
rs73546873	1.00[ASN][1000 genomes]
rs9804577	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533794	chr11:107349817-108093259	Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv1039425	chr11:107468681-107895836	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv427899	chr11:107471544-107805894	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv1049524	chr11:107540937-107954011	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv1038581	chr11:107564274-107838386	Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv898378	chr11:107580985-107847983	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv521771	chr11:107590335-107904646	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases
8	nsv1048938	chr11:107604473-107929950	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases
9	nsv1035229	chr11:107653731-107717190	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
10	nsv1052829	chr11:107686808-107725297	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv1045388	chr11:107686808-107733498	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
12	esv3417743	chr11:107699670-107725103	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107673400-107727800	Weak transcription	Primary B cells from cord blood	blood
2	chr11:107691200-107709600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:107696600-107711000	Weak transcription	Primary B cells from peripheral blood	blood
4	chr11:107697200-107702200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr11:107697200-107709800	Weak transcription	GM12878-XiMat	blood
6	chr11:107701400-107702200	Enhancers	Liver	Liver
7	chr11:107701400-107702200	Enhancers	Stomach Mucosa	stomach
8	chr11:107701400-107702200	Enhancers	A549	lung
9	chr11:107701400-107702600	Enhancers	Hela-S3	cervix
10	chr11:107701400-107703000	Enhancers	HUVEC	blood vessel
11	chr11:107701400-107703800	Enhancers	HMEC	breast
12	chr11:107701400-107704000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:107701400-107704000	Enhancers	NHEK	skin
14	chr11:107701400-107704400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:107701600-107704400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr11:107701800-107702200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr11:107701800-107703600	Enhancers	K562	blood
18	chr11:107702000-107702400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr11:107702000-107702400	Enhancers	Gastric	stomach
20	chr11:107702000-107702400	Enhancers	Pancreas	Pancrea
21	chr11:107702000-107702600	Enhancers	Esophagus	oesophagus

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