Variant report

Variant	nsv609731
Chromosome Location	chr8:3181378-3182062
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:100 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs156071	chr8:3181378-3181379	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200121626	chr8:3181384-3181385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374475958	chr8:3181392-3181393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146647608	chr8:3181400-3181401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201194359	chr8:3181416-3181417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75216556	chr8:3181423-3181424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371271721	chr8:3181431-3181432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577968038	chr8:3181433-3181434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77130980	chr8:3181440-3181441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537383144	chr8:3181443-3181444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs79330555	chr8:3181450-3181451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75755353	chr8:3181452-3181453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs5888962	chr8:3181455-3181456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs79812545	chr8:3181457-3181458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374216148	chr8:3181462-3181463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533146608	chr8:3181471-3181472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368034848	chr8:3181490-3181491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372172290	chr8:3181492-3181493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111336467	chr8:3181494-3181495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551044448	chr8:3181501-3181502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs201343296	chr8:3181502-3181503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112360870	chr8:3181503-3181504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112761323	chr8:3181511-3181512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542689765	chr8:3181513-3181514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113059239	chr8:3181521-3181522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35998459	chr8:3181526-3181527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113641381	chr8:3181527-3181528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs202209876	chr8:3181533-3181534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561399631	chr8:3181534-3181535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200569867	chr8:3181543-3181544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201484656	chr8:3181566-3181567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528580939	chr8:3181572-3181573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs113842215	chr8:3181573-3181574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs61408962	chr8:3181574-3181575	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs536113125	chr8:3181575-3181576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs71502954	chr8:3181583-3181584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571500230	chr8:3181586-3181587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532615695	chr8:3181591-3181592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371433297	chr8:3181593-3181594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76451761	chr8:3181595-3181596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550177303	chr8:3181597-3181598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200627725	chr8:3181600-3181601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550843156	chr8:3181610-3181611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569486363	chr8:3181611-3181612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs13274025	chr8:3181613-3181614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536789976	chr8:3181614-3181615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537019060	chr8:3181624-3181625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548727896	chr8:3181627-3181628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188563078	chr8:3181628-3181629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2406353	chr8:3181631-3181632	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	19805367	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
early-passage human iPS cells	21368824	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:3180000-3182000	Enhancers	Primary B cells from peripheral blood	blood

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