Variant report

Variant	esv2109329
Chromosome Location	chr8:11796835-11797229
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11662199..11664746-chr8:11796348..11798802,2	K562	blood:

Extended variants
information (count: 35 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376751435	chr8:11796853-11796854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs375435586	chr8:11796854-11796855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148544405	chr8:11796861-11796862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146203235	chr8:11796899-11796900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191102625	chr8:11796906-11796907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536210809	chr8:11796907-11796908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs117031054	chr8:11796927-11796928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183325461	chr8:11796958-11796959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187668088	chr8:11796965-11796966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564745274	chr8:11796972-11796973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576581568	chr8:11796973-11796974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192881013	chr8:11796986-11796987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183486686	chr8:11796989-11796990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13275143	chr8:11796990-11796991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs548544925	chr8:11796996-11796997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369288862	chr8:11797010-11797011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558327440	chr8:11797013-11797014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375960400	chr8:11797017-11797018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563875117	chr8:11797019-11797020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531224723	chr8:11797023-11797024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143387422	chr8:11797030-11797031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368620143	chr8:11797045-11797046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200640534	chr8:11797049-11797050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373269719	chr8:11797050-11797051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571060626	chr8:11797053-11797054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs57159956	chr8:11797068-11797069	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs58869268	chr8:11797095-11797096	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs565745797	chr8:11797108-11797109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535914166	chr8:11797109-11797110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs114355980	chr8:11797128-11797129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575907487	chr8:11797148-11797149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147964689	chr8:11797149-11797150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187983292	chr8:11797167-11797168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558400176	chr8:11797173-11797174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs57356272	chr8:11797180-11797181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:139)

Disease	PMID	Source
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
Prostate cancer	16573809	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
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11786000-11799400	Weak transcription	Right Atrium	heart
2	chr8:11794200-11798800	Weak transcription	Stomach Mucosa	stomach

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