Variant report

Variant	nsv606263
Chromosome Location	chr7:13590568-13591131
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116501616	chr7:13590604-13590605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147788388	chr7:13590633-13590634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543405877	chr7:13590652-13590653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563579440	chr7:13590660-13590661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562174183	chr7:13590674-13590675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529351127	chr7:13590711-13590712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572844790	chr7:13590743-13590744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs367606847	chr7:13590749-13590750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs116031434	chr7:13590771-13590772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559319804	chr7:13590774-13590775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs528267823	chr7:13590779-13590780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547597757	chr7:13590792-13590793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570883151	chr7:13590812-13590813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs12699533	chr7:13590851-13590852	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs77454972	chr7:13590873-13590874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535778650	chr7:13590896-13590897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1880633	chr7:13590910-13590911	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs572570970	chr7:13590978-13590979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561393781	chr7:13590986-13590987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115184264	chr7:13590988-13590989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530043378	chr7:13591003-13591004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369878396	chr7:13591036-13591037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192799233	chr7:13591065-13591066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566970104	chr7:13591094-13591095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1880632	chr7:13591095-13591096	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs563314879	chr7:13591109-13591110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs36100395	chr7:13591117-13591118	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13590600-13591400	Enhancers	Psoas Muscle	Psoas
2	chr7:13590800-13591600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:13590800-13592000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:13591000-13591800	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr7:13591000-13592000	Enhancers	HSMMtube	muscle

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