Variant report

Variant	esv20481
Chromosome Location	chr8:119445015-119446781
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:67 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566764526	chr8:119445019-119445020	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs527883220	chr8:119445040-119445041	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568835717	chr8:119445064-119445065	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs9643128	chr8:119445101-119445102	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs538121260	chr8:119445133-119445134	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs9643129	chr8:119445141-119445142	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs571213977	chr8:119445148-119445149	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181243289	chr8:119445171-119445172	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553892838	chr8:119445287-119445288	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs9642841	chr8:119445360-119445361	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs9643130	chr8:119445380-119445381	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs553883136	chr8:119445401-119445402	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554435038	chr8:119445503-119445504	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576310245	chr8:119445561-119445562	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184211359	chr8:119445562-119445563	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562554026	chr8:119445592-119445593	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376378836	chr8:119445597-119445598	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188891369	chr8:119445628-119445629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs13439537	chr8:119445649-119445650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs200881997	chr8:119445651-119445652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs386413795	chr8:119445661-119445662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs367554291	chr8:119445663-119445664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201675896	chr8:119445664-119445665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560191518	chr8:119445678-119445679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527913320	chr8:119445685-119445686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs549568708	chr8:119445705-119445706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12679878	chr8:119445719-119445720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561294212	chr8:119445749-119445750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs12679866	chr8:119445776-119445777	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs7812733	chr8:119445879-119445880	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs571301631	chr8:119445887-119445888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375992131	chr8:119445889-119445890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538618616	chr8:119445937-119445938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7812880	chr8:119445980-119445981	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs7813116	chr8:119445998-119445999	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs535940507	chr8:119446009-119446010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181811653	chr8:119446027-119446028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576118069	chr8:119446037-119446038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7831361	chr8:119446102-119446103	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs533358445	chr8:119446140-119446141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147356470	chr8:119446155-119446156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577643018	chr8:119446157-119446158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376616141	chr8:119446165-119446166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369100099	chr8:119446179-119446180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560079145	chr8:119446183-119446184	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73708490	chr8:119446189-119446190	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs7813395	chr8:119446196-119446197	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs7831501	chr8:119446209-119446210	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs531799889	chr8:119446256-119446257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs115405926	chr8:119446292-119446293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:142)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119434800-119451800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:119438000-119446400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:119442200-119449200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:119443800-119445400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:119445000-119445200	Enhancers	Aorta	Aorta
6	chr8:119445000-119445600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr8:119445200-119445400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr8:119445200-119445600	Weak transcription	Aorta	Aorta
9	chr8:119445200-119445600	Enhancers	HUVEC	blood vessel
10	chr8:119445200-119445800	Enhancers	NHLF	lung
11	chr8:119445200-119446000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:119445200-119446000	Enhancers	NHDF-Ad	bronchial
13	chr8:119445200-119446200	Enhancers	Osteobl	bone
14	chr8:119445200-119446800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr8:119445400-119445600	ZNF genes & repeats	Fetal Intestine Small	intestine
16	chr8:119445400-119445800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr8:119445400-119448600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr8:119445600-119445800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr8:119445600-119446200	Weak transcription	Fetal Intestine Small	intestine
20	chr8:119445600-119448000	Weak transcription	HUVEC	blood vessel
21	chr8:119445600-119450600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr8:119445800-119446200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:119445800-119446200	Weak transcription	NHLF	lung
24	chr8:119446000-119446200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr8:119446000-119446800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr8:119446000-119447000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr8:119446000-119450000	Weak transcription	NHDF-Ad	bronchial
28	chr8:119446000-119450800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:119446200-119446400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:119446200-119446400	Enhancers	NHLF	lung
31	chr8:119446200-119446800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr8:119446200-119450400	Weak transcription	Osteobl	bone
33	chr8:119446400-119447000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:119446400-119449600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr8:119446400-119450400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:119446400-119451000	Weak transcription	NHLF	lung

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