Variant report

Variant	esv3529893
Chromosome Location	chr8:63782719-63783358
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:45 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13248017	chr8:63782768-63782769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs13280676	chr8:63782773-63782774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372577780	chr8:63782774-63782775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555591945	chr8:63782776-63782777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367788453	chr8:63782785-63782786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182066148	chr8:63782788-63782789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538116849	chr8:63782791-63782792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372938683	chr8:63782800-63782801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370536390	chr8:63782810-63782811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200367307	chr8:63782815-63782816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77272732	chr8:63782818-63782819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs13280738	chr8:63782833-63782834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76292198	chr8:63782835-63782836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371578257	chr8:63782840-63782841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577886006	chr8:63782847-63782848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369491023	chr8:63782849-63782850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377267932	chr8:63782853-63782854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373467521	chr8:63782857-63782858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34256635	chr8:63782886-63782887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545853585	chr8:63782933-63782934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564506248	chr8:63782936-63782937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573213141	chr8:63782939-63782940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558411394	chr8:63782950-63782951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186300225	chr8:63782954-63782955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369418640	chr8:63783006-63783007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561940120	chr8:63783041-63783042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529471726	chr8:63783042-63783043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112894603	chr8:63783119-63783120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs55919106	chr8:63783141-63783142	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs28535037	chr8:63783198-63783199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576677650	chr8:63783211-63783212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs28638109	chr8:63783214-63783215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4260888	chr8:63783217-63783218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4457325	chr8:63783232-63783233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551049274	chr8:63783238-63783239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566503397	chr8:63783240-63783241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs55797491	chr8:63783246-63783247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs56332837	chr8:63783250-63783251	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs56036420	chr8:63783256-63783257	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs538006401	chr8:63783258-63783259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189856352	chr8:63783268-63783269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556418018	chr8:63783295-63783296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571407898	chr8:63783302-63783303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28730420	chr8:63783305-63783306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs56266890	chr8:63783329-63783330	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
Salivary gland tumor	18059337	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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63782000-63792200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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