Variant report

Variant	esv3400012
Chromosome Location	chr4:91563028-91563465
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539232597	chr4:91563037-91563038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs565866296	chr4:91563044-91563045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs13126128	chr4:91563055-91563056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13126314	chr4:91563056-91563057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536183411	chr4:91563063-91563064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548485522	chr4:91563077-91563078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552857790	chr4:91563096-91563097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370084508	chr4:91563107-91563108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116113695	chr4:91563137-91563138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569815516	chr4:91563155-91563156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528865546	chr4:91563195-91563196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555741239	chr4:91563204-91563205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12642596	chr4:91563214-91563215	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs544764284	chr4:91563255-91563256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115690151	chr4:91563281-91563282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs578233896	chr4:91563290-91563291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558474917	chr4:91563324-91563325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570655868	chr4:91563364-91563365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534782278	chr4:91563379-91563380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113577650	chr4:91563391-91563392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529596833	chr4:91563415-91563416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1039146	chr4:91563456-91563457	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Obesity	20622171	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Esophageal adenocarcinoma	18519675	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91550800-91564400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:91550800-91566800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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