Variant report

Variant	rs11033034
Chromosome Location	chr11:35258330-35258331
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:35256103..35261501-chr11:35384186..35388588,8	MCF-7	breast:
2	chr11:35249750..35251832-chr11:35258171..35261119,2	K562	blood:
3	chr11:35258018..35260931-chr11:35412299..35415204,2	MCF-7	breast:
4	chr11:35253589..35256594-chr11:35257104..35259626,3	MCF-7	breast:

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10488813	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10836347	0.86[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs10836349	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10836352	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10836353	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10836358	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11033031	0.89[EUR][1000 genomes]
rs11033039	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11033041	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11033042	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11033043	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12360706	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12364027	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12575005	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1570216	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3812778	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3829280	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4503504	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4508184	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs55715534	0.81[EUR][1000 genomes]
rs56193087	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs67384276	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7104662	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7122374	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72638195	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72916162	0.81[EUR][1000 genomes]

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	nsv1045837	chr11:34893992-35395190	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv541003	chr11:35122694-35261451	Genic enhancers Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv541004	chr11:35122694-35297414	Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv897218	chr11:35241989-35261374	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	nsv897220	chr11:35242907-35261374	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
6	nsv897221	chr11:35242907-35265444	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
7	nsv897222	chr11:35244044-35261374	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35233400-35259600	Weak transcription	Liver	Liver
2	chr11:35236800-35259600	Weak transcription	Psoas Muscle	Psoas
3	chr11:35237000-35259600	Weak transcription	HUVEC	blood vessel
4	chr11:35241200-35259600	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr11:35245400-35259600	Weak transcription	Brain Hippocampus Middle	brain
6	chr11:35247000-35263200	Weak transcription	HSMMtube	muscle
7	chr11:35251400-35259400	Weak transcription	Left Ventricle	heart
8	chr11:35251400-35259800	Weak transcription	Gastric	stomach
9	chr11:35252200-35259400	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr11:35252400-35258600	Weak transcription	Fetal Lung	lung
11	chr11:35252400-35259400	Weak transcription	Lung	lung
12	chr11:35253000-35259400	Weak transcription	Adipose Nuclei	Adipose
13	chr11:35253000-35260400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr11:35253400-35259400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr11:35254000-35259400	Weak transcription	Brain Substantia Nigra	brain
16	chr11:35254600-35264000	Weak transcription	Colon Smooth Muscle	Colon
17	chr11:35254600-35264000	Weak transcription	NHLF	lung
18	chr11:35255400-35266800	Weak transcription	Stomach Smooth Muscle	stomach
19	chr11:35255600-35259600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr11:35255600-35260800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr11:35255800-35258800	Enhancers	Dnd41	blood
22	chr11:35256400-35258600	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr11:35256400-35258800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr11:35256600-35258400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr11:35256600-35258600	Enhancers	HMEC	breast
26	chr11:35256600-35258800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr11:35256600-35259800	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr11:35256600-35260000	Enhancers	NHEK	skin
29	chr11:35256600-35260200	Enhancers	Primary T cells fromperipheralblood	blood
30	chr11:35256600-35260200	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr11:35256600-35260200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr11:35256600-35260400	Enhancers	Primary T cells from cord blood	blood
33	chr11:35256600-35260400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr11:35256600-35261200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr11:35256800-35258600	Enhancers	Hela-S3	cervix
36	chr11:35256800-35258800	Enhancers	NH-A	brain
37	chr11:35256800-35260000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr11:35256800-35260600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr11:35257000-35258600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr11:35257000-35258600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr11:35257000-35260000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr11:35257200-35258400	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr11:35257200-35258800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr11:35257400-35258400	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr11:35257400-35258600	Enhancers	Stomach Mucosa	stomach
46	chr11:35257400-35258800	Enhancers	NHDF-Ad	bronchial
47	chr11:35257400-35260200	Enhancers	Fetal Thymus	thymus
48	chr11:35257400-35261800	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr11:35257600-35258400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr11:35257600-35258400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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