Variant report

Variant	esv3343092
Chromosome Location	chr7:14450577-14452475
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549061633	chr7:14452000-14452001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs74991282	chr7:14452030-14452031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149999554	chr7:14452053-14452054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557188030	chr7:14452097-14452098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554071653	chr7:14452118-14452119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183648608	chr7:14452119-14452120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539707805	chr7:14452132-14452133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556290687	chr7:14452186-14452187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576336921	chr7:14452217-14452218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147705230	chr7:14452230-14452231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10239634	chr7:14452244-14452245	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs117580122	chr7:14452280-14452281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541251745	chr7:14452289-14452290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116839044	chr7:14452319-14452320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533275055	chr7:14452326-14452327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543655106	chr7:14452327-14452328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142513092	chr7:14452343-14452344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528873651	chr7:14452344-14452345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569456792	chr7:14452345-14452346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367560040	chr7:14452349-14452350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10242702	chr7:14452358-14452359	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs528931779	chr7:14452379-14452380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146832065	chr7:14452391-14452392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375132290	chr7:14452397-14452398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570668399	chr7:14452401-14452402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs139257650	chr7:14452405-14452406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs12539016	chr7:14452470-14452471	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs569989512	chr7:14452473-14452474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535820935	chr7:14452475-14452476	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
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
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
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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21645411	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14452000-14452800	Enhancers	Fetal Heart	heart

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