Variant report

Variant	esv3387177
Chromosome Location	chr8:1575963-1576468
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:57 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551382719	chr8:1575964-1575965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564709908	chr8:1575978-1575979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527418935	chr8:1575988-1575989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570984469	chr8:1575990-1575991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35469943	chr8:1576010-1576011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535203148	chr8:1576019-1576020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs36103948	chr8:1576030-1576031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4875879	chr8:1576047-1576048	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567472037	chr8:1576062-1576063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536410610	chr8:1576068-1576069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550113919	chr8:1576069-1576070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111471507	chr8:1576071-1576072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113717326	chr8:1576082-1576083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs60802086	chr8:1576088-1576089	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs112814148	chr8:1576104-1576105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111476284	chr8:1576114-1576115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113157706	chr8:1576120-1576121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558167893	chr8:1576121-1576122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113895945	chr8:1576123-1576124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112041655	chr8:1576134-1576135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577949931	chr8:1576140-1576141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535901148	chr8:1576143-1576144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs56118974	chr8:1576147-1576148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534350880	chr8:1576152-1576153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4875880	chr8:1576156-1576157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113041350	chr8:1576163-1576164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201330223	chr8:1576167-1576168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573908740	chr8:1576175-1576176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4875881	chr8:1576186-1576187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542780477	chr8:1576192-1576193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112357525	chr8:1576208-1576209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369588513	chr8:1576213-1576214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148011074	chr8:1576216-1576217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545364728	chr8:1576224-1576225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13264267	chr8:1576225-1576226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs55803714	chr8:1576244-1576245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112713012	chr8:1576255-1576256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564939644	chr8:1576260-1576261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112808049	chr8:1576268-1576269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139128492	chr8:1576270-1576271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113776265	chr8:1576290-1576291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112040022	chr8:1576312-1576313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71516202	chr8:1576322-1576323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79858136	chr8:1576328-1576329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560930102	chr8:1576336-1576337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75393278	chr8:1576342-1576343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111841215	chr8:1576359-1576360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112040927	chr8:1576380-1576381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550028531	chr8:1576383-1576384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547014163	chr8:1576394-1576395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	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
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	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
Breast cancer	21364760	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
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1570400-1579800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr8:1575200-1599400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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