Variant report

Variant	nsv971315
Chromosome Location	chr8:63873161-63874923
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:79 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527777026	chr8:63873163-63873164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs10093652	chr8:63873199-63873200	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs567437404	chr8:63873209-63873210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538026455	chr8:63873210-63873211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556746205	chr8:63873275-63873276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146286673	chr8:63873282-63873283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200379215	chr8:63873293-63873294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201453222	chr8:63873294-63873295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539361555	chr8:63873296-63873297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs60452313	chr8:63873316-63873317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557141913	chr8:63873334-63873335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186659246	chr8:63873355-63873356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553487895	chr8:63873396-63873397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs72656543	chr8:63873397-63873398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191162649	chr8:63873421-63873422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184039192	chr8:63873432-63873433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576223198	chr8:63873433-63873434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543229160	chr8:63873444-63873445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200224473	chr8:63873470-63873471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114002192	chr8:63873490-63873491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139295957	chr8:63873498-63873499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572549922	chr8:63873510-63873511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112665219	chr8:63873548-63873549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186946721	chr8:63873560-63873561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112914329	chr8:63873561-63873562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548987379	chr8:63873604-63873605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567400797	chr8:63873620-63873621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142572137	chr8:63873625-63873626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544593873	chr8:63873664-63873665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534089156	chr8:63873669-63873670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550100165	chr8:63873670-63873671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145955363	chr8:63873745-63873746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367576468	chr8:63873764-63873765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554467367	chr8:63873768-63873769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566389287	chr8:63873771-63873772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536223819	chr8:63873776-63873777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554630898	chr8:63873803-63873804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7846151	chr8:63873843-63873844	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs77292554	chr8:63873852-63873853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543543157	chr8:63873853-63873854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139528063	chr8:63873888-63873889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576923364	chr8:63873929-63873930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558754926	chr8:63873934-63873935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113930017	chr8:63873972-63873973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540876731	chr8:63873975-63873976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543941630	chr8:63874002-63874003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200579093	chr8:63874050-63874051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577026984	chr8:63874115-63874116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149657811	chr8:63874126-63874127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548397074	chr8:63874147-63874148	Weak transcription	n/a	n/a	Overlapped CNVs	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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63859600-63877800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:63868600-63895800	Weak transcription	Fetal Brain Female	brain
3	chr8:63871800-63875400	Weak transcription	Placenta	Placenta

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