Variant report

Variant	esv1842111
Chromosome Location	chr5:45363063-45373943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1392971	chr5:45363063-45363064	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547695502	chr5:45363093-45363094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572247647	chr5:45363117-45363118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs532428254	chr5:45363168-45363169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200592797	chr5:45363235-45363236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs202188356	chr5:45363246-45363247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376462762	chr5:45363247-45363248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370714390	chr5:45363248-45363249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs34074894	chr5:45363268-45363269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184542434	chr5:45363322-45363323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368149234	chr5:45363324-45363325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570692678	chr5:45363386-45363387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553963438	chr5:45363462-45363463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375674038	chr5:45363481-45363482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576944349	chr5:45363483-45363484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372396778	chr5:45363497-45363498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142731016	chr5:45363511-45363512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189052723	chr5:45363539-45363540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531587297	chr5:45363592-45363593	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hirschsprung''s Disease	21712996	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:45361600-45363400	Weak transcription	Pancreas	Pancrea
2	chr5:45363400-45363600	Enhancers	Pancreas	Pancrea

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