Variant report

Variant	rs11850711
Chromosome Location	chr14:64377908-64377909
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	chr14:64372158..64375131-chr14:64377283..64378855,2	MCF-7	breast:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11158519	0.86[MEX][hapmap]
rs11158520	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12588807	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12589453	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12878037	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12878348	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12879374	0.80[AMR][1000 genomes]
rs12881942	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12882429	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12888489	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12888712	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12894963	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12896120	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17751301	1.00[CEU][hapmap]
rs17824268	1.00[CEU][hapmap]
rs33976862	1.00[CEU][hapmap];0.83[GIH][hapmap];1.00[MEX][hapmap]
rs34328391	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34556545	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35009554	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35984502	0.80[AMR][1000 genomes]
rs3818774	0.89[AMR][1000 genomes]
rs4459477	0.87[CEU][hapmap];0.86[MEX][hapmap]
rs4899120	0.87[CEU][hapmap]
rs6573539	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs71416319	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8015210	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915909	chr14:63620440-64560369	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1038825	chr14:64109441-64491720	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv1037140	chr14:64248421-64442980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv542119	chr14:64248421-64442980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv564904	chr14:64346190-64416898	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	esv1793389	chr14:64346190-64457224	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64337800-64403800	Weak transcription	Thymus	Thymus
2	chr14:64360600-64382200	Weak transcription	Psoas Muscle	Psoas
3	chr14:64364400-64385200	Weak transcription	Pancreas	Pancrea
4	chr14:64364600-64387800	Weak transcription	HMEC	breast
5	chr14:64365000-64430200	Weak transcription	Fetal Brain Male	brain
6	chr14:64365200-64386200	Weak transcription	Gastric	stomach
7	chr14:64365400-64379800	Weak transcription	Fetal Thymus	thymus
8	chr14:64365400-64393600	Weak transcription	Right Ventricle	heart
9	chr14:64367400-64378000	Weak transcription	Primary B cells from peripheral blood	blood
10	chr14:64369800-64386200	Weak transcription	Esophagus	oesophagus
11	chr14:64372200-64378000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr14:64374600-64399600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr14:64375200-64385000	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr14:64375200-64395000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr14:64375200-64395200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr14:64375400-64380000	Strong transcription	Dnd41	blood
17	chr14:64375600-64381000	Weak transcription	NHEK	skin
18	chr14:64375800-64378000	Enhancers	Muscle Satellite Cultured Cells	--
19	chr14:64375800-64378400	Weak transcription	Colonic Mucosa	Colon
20	chr14:64375800-64380800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr14:64375800-64381000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr14:64375800-64384000	Weak transcription	Fetal Intestine Large	intestine
23	chr14:64375800-64384800	Weak transcription	Fetal Kidney	kidney
24	chr14:64375800-64386200	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr14:64375800-64388600	Weak transcription	Hela-S3	cervix
26	chr14:64375800-64389000	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr14:64375800-64393200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr14:64376000-64378000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr14:64376000-64378000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr14:64376000-64378000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr14:64376000-64378000	Enhancers	NHDF-Ad	bronchial
32	chr14:64376000-64378200	Enhancers	NHLF	lung
33	chr14:64376000-64383400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr14:64376000-64385400	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr14:64376000-64386200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr14:64376000-64386200	Weak transcription	Left Ventricle	heart
37	chr14:64376000-64389000	Weak transcription	Adipose Nuclei	Adipose
38	chr14:64376000-64389600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr14:64376000-64389600	Weak transcription	Duodenum Mucosa	Duodenum
40	chr14:64376000-64389600	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr14:64376000-64391200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr14:64376000-64399200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr14:64376000-64399600	Weak transcription	Small Intestine	intestine
44	chr14:64376000-64399800	Weak transcription	Primary T cells from cord blood	blood
45	chr14:64376000-64416200	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr14:64376200-64379800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr14:64376200-64399400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr14:64376400-64378200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr14:64376400-64378400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
50	chr14:64376400-64380600	Strong transcription	Primary T cells fromperipheralblood	blood

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