Variant report

Variant	rs11212391
Chromosome Location	chr11:107694914-107694915
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:107693680..107695656-chr11:107699193..107701857,2	MCF-7	breast:
2	chr11:107693861..107695588-chr11:107701609..107703172,2	K562	blood:
3	chr11:107691036..107695039-chr11:107696173..107700652,4	K562	blood:

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10890764	1.00[EUR][1000 genomes]
rs11212379	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11212383	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11212389	1.00[EUR][1000 genomes]
rs11212390	1.00[EUR][1000 genomes]
rs11212392	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11212393	1.00[EUR][1000 genomes]
rs11212394	1.00[EUR][1000 genomes]
rs11212395	1.00[EUR][1000 genomes]
rs11212396	1.00[EUR][1000 genomes]
rs11212397	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11212398	1.00[EUR][1000 genomes]
rs11212400	1.00[EUR][1000 genomes]
rs12098896	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12099368	1.00[EUR][1000 genomes]
rs12099420	0.82[EUR][1000 genomes]
rs12146456	1.00[EUR][1000 genomes]
rs12146459	1.00[EUR][1000 genomes]
rs12270982	0.91[EUR][1000 genomes]
rs12271120	1.00[EUR][1000 genomes]
rs12278904	1.00[EUR][1000 genomes]
rs12279264	0.95[EUR][1000 genomes]
rs12281160	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12288093	1.00[EUR][1000 genomes]
rs12291200	1.00[EUR][1000 genomes]
rs12292050	1.00[EUR][1000 genomes]
rs12292254	1.00[EUR][1000 genomes]
rs12293650	1.00[EUR][1000 genomes]
rs57429831	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58124926	0.95[EUR][1000 genomes]
rs59036211	1.00[EUR][1000 genomes]
rs60539601	0.95[EUR][1000 genomes]
rs66625589	1.00[EUR][1000 genomes]
rs67596776	0.95[EUR][1000 genomes]
rs7118580	1.00[EUR][1000 genomes]
rs7120382	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72999546	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73001540	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73001542	0.81[EUR][1000 genomes]
rs73001547	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73001550	1.00[EUR][1000 genomes]
rs73001554	1.00[EUR][1000 genomes]
rs73001562	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73001563	1.00[EUR][1000 genomes]
rs73001566	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73003327	1.00[EUR][1000 genomes]
rs73003344	1.00[EUR][1000 genomes]
rs73003346	1.00[EUR][1000 genomes]
rs73003355	1.00[EUR][1000 genomes]
rs73003360	1.00[EUR][1000 genomes]
rs73003382	1.00[EUR][1000 genomes]
rs73003384	1.00[EUR][1000 genomes]
rs73005370	0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 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	nsv468867	chr11:107649026-107697633	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
10	nsv556382	chr11:107649026-107697633	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
11	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
12	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
13	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

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107672000-107697000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr11:107673400-107727800	Weak transcription	Primary B cells from cord blood	blood
3	chr11:107679000-107696400	Weak transcription	Lung	lung
4	chr11:107682600-107695200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:107682600-107695400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:107683400-107701600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr11:107684800-107695200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr11:107685600-107695400	Weak transcription	Primary B cells from peripheral blood	blood
9	chr11:107690200-107695200	Weak transcription	GM12878-XiMat	blood
10	chr11:107690600-107695000	Weak transcription	HMEC	breast
11	chr11:107690600-107701400	Weak transcription	A549	lung
12	chr11:107691200-107709600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr11:107692600-107695200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr11:107692600-107695400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr11:107692600-107697400	Enhancers	HUVEC	blood vessel
16	chr11:107692600-107701800	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr11:107693000-107695200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr11:107693600-107695200	Weak transcription	NHEK	skin
19	chr11:107694200-107695000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr11:107694600-107695000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links