Variant report

Variant	rs2785191
Chromosome Location	chr11:35104432-35104433
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	chr11:35104262..35106718-chr11:35159601..35161198,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000026508	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11523460	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1365057	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2093663	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2248428	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2553818	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs2553822	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2553823	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2553824	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2732534	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2732535	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2785188	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs890239	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs890240	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[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	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	nsv430371	chr11:34975067-35111292	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv540999	chr11:35021936-35185471	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	esv2758263	chr11:35029933-35226784	Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	esv2759818	chr11:35029933-35238578	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
6	nsv541000	chr11:35053717-35185471	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
7	nsv541001	chr11:35053717-35224624	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
8	esv2757437	chr11:35067482-35238578	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' 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 target site	27 gene(s)	inside rSNPs	diseases
9	esv2752912	chr11:35074167-35238578	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers 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	27 gene(s)	inside rSNPs	diseases
10	nsv508623	chr11:35094933-35203363	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
11	nsv541002	chr11:35101282-35224624	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
12	nsv975326	chr11:35103908-35125981	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35097600-35106400	Enhancers	Primary B cells from peripheral blood	blood
2	chr11:35097800-35106600	Enhancers	Fetal Thymus	thymus
3	chr11:35098800-35105400	Weak transcription	Small Intestine	intestine
4	chr11:35103200-35104800	Enhancers	NHDF-Ad	bronchial
5	chr11:35103200-35106600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:35103200-35106800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr11:35103200-35107800	Enhancers	Adipose Nuclei	Adipose
8	chr11:35103200-35110600	Enhancers	Fetal Muscle Leg	muscle
9	chr11:35103400-35104800	Enhancers	Spleen	Spleen
10	chr11:35103400-35105400	Enhancers	Pancreas	Pancrea
11	chr11:35103400-35106600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr11:35103600-35105400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr11:35103600-35105600	Enhancers	Placenta	Placenta
14	chr11:35103600-35106800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr11:35103600-35108400	Enhancers	Fetal Muscle Trunk	muscle
16	chr11:35103800-35104600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr11:35103800-35104600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
18	chr11:35103800-35104600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
19	chr11:35103800-35104600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
20	chr11:35103800-35104600	Enhancers	HSMMtube	muscle
21	chr11:35103800-35104800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:35103800-35104800	Enhancers	Right Atrium	heart
23	chr11:35103800-35104800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr11:35103800-35105000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr11:35103800-35105000	Flanking Active TSS	Duodenum Mucosa	Duodenum
26	chr11:35103800-35105000	Flanking Active TSS	HMEC	breast
27	chr11:35103800-35105200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
28	chr11:35103800-35105200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:35103800-35105200	Enhancers	Left Ventricle	heart
30	chr11:35103800-35105200	Enhancers	Placenta Amnion	Placenta Amnion
31	chr11:35103800-35105200	Enhancers	Right Ventricle	heart
32	chr11:35103800-35105200	Flanking Active TSS	Osteobl	bone
33	chr11:35103800-35105400	Flanking Active TSS	Primary T cells from cord blood	blood
34	chr11:35103800-35105400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
35	chr11:35103800-35105400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
36	chr11:35103800-35105400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
37	chr11:35103800-35105400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
38	chr11:35103800-35105400	Enhancers	Brain Cingulate Gyrus	brain
39	chr11:35103800-35105400	Enhancers	Colon Smooth Muscle	Colon
40	chr11:35103800-35105400	Enhancers	Esophagus	oesophagus
41	chr11:35103800-35105400	Enhancers	Lung	lung
42	chr11:35103800-35105400	Flanking Active TSS	Hela-S3	cervix
43	chr11:35103800-35105400	Flanking Active TSS	NHEK	skin
44	chr11:35103800-35105600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
45	chr11:35103800-35105600	Enhancers	Brain Anterior Caudate	brain
46	chr11:35103800-35105600	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr11:35103800-35105600	Enhancers	K562	blood
48	chr11:35103800-35105800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr11:35103800-35105800	Flanking Active TSS	GM12878-XiMat	blood
50	chr11:35103800-35106000	Enhancers	Primary neutrophils fromperipheralblood	blood

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