Variant report

Variant	nsv562067
Chromosome Location	chr13:65350465-65353382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:89 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151019144	chr13:65351208-65351209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs187933069	chr13:65351250-65351251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs193242459	chr13:65351326-65351327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34782093	chr13:65351347-65351348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138557569	chr13:65351349-65351350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs71103162	chr13:65351369-65351370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76860154	chr13:65351370-65351371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537350897	chr13:65351371-65351372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140842935	chr13:65351372-65351373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141093404	chr13:65351398-65351399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530113027	chr13:65351413-65351414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546725383	chr13:65351429-65351430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116255226	chr13:65351462-65351463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144855295	chr13:65351537-65351538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552794382	chr13:65351590-65351591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569440124	chr13:65351630-65351631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555762985	chr13:65351654-65351655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373315342	chr13:65351666-65351667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558207957	chr13:65351667-65351668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201625260	chr13:65351673-65351674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146727873	chr13:65351784-65351785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140316598	chr13:65351790-65351791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574104036	chr13:65351812-65351813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567302453	chr13:65351823-65351824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185398449	chr13:65351837-65351838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189464330	chr13:65351900-65351901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192210450	chr13:65351902-65351903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544887507	chr13:65351909-65351910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145395045	chr13:65351910-65351911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575448250	chr13:65351913-65351914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs137976313	chr13:65351929-65351930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561112023	chr13:65351965-65351966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530052708	chr13:65352006-65352007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577310250	chr13:65352103-65352104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149466010	chr13:65352117-65352118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7995434	chr13:65352131-65352132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs552492719	chr13:65352167-65352168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569461395	chr13:65352187-65352188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143014354	chr13:65352270-65352271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs148185665	chr13:65352283-65352284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567239282	chr13:65352304-65352305	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143334126	chr13:65352325-65352326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147526291	chr13:65352339-65352340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77451945	chr13:65352364-65352365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140089323	chr13:65352404-65352405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs539885211	chr13:65352415-65352416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575430602	chr13:65352431-65352432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs74965325	chr13:65352469-65352470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575594090	chr13:65352470-65352471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75450049	chr13:65352481-65352482	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65351200-65353200	Enhancers	HUVEC	blood vessel
2	chr13:65352200-65352600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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