Variant report

Variant	esv3337041
Chromosome Location	chr7:14267950-14268363
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372068915	chr7:14267961-14267962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs188542474	chr7:14268010-14268011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149549626	chr7:14268013-14268014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575232184	chr7:14268022-14268023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372877690	chr7:14268033-14268034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs377112726	chr7:14268062-14268063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs566010787	chr7:14268081-14268082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143242527	chr7:14268113-14268114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557560684	chr7:14268124-14268125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548570123	chr7:14268127-14268128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148322283	chr7:14268140-14268141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543300510	chr7:14268162-14268163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534957426	chr7:14268163-14268164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs62445579	chr7:14268168-14268169	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs10264420	chr7:14268193-14268194	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs143157664	chr7:14268197-14268198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530887557	chr7:14268223-14268224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73679694	chr7:14268244-14268245	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs375649047	chr7:14268261-14268262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368145557	chr7:14268272-14268273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147503817	chr7:14268305-14268306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529942369	chr7:14268317-14268318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546537574	chr7:14268318-14268319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs193148736	chr7:14268349-14268350	Weak transcription	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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14250000-14273400	Weak transcription	Left Ventricle	heart
2	chr7:14267400-14272400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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