Variant report

Variant	nsv979832
Chromosome Location	chr3:51910868-51912640
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 86 )

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	rs12637540	chr3:51910870-51910871	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs79370141	chr3:51910873-51910874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553903119	chr3:51910890-51910891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140593252	chr3:51910947-51910948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376994964	chr3:51911002-51911003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563448413	chr3:51911022-51911023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs190316271	chr3:51911040-51911041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192562621	chr3:51911057-51911058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563933910	chr3:51911102-51911103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201734789	chr3:51911104-51911105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552372174	chr3:51911108-51911109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550161245	chr3:51911113-51911114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369711148	chr3:51911114-51911115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs199970040	chr3:51911115-51911116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142612817	chr3:51911116-51911117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199649050	chr3:51911117-51911118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561442178	chr3:51911118-51911119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528040015	chr3:51911123-51911124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs71297379	chr3:51911141-51911142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183680544	chr3:51911164-51911165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566398140	chr3:51911186-51911187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569183675	chr3:51911210-51911211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112886560	chr3:51911261-51911262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145676275	chr3:51911320-51911321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188294525	chr3:51911333-51911334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554965469	chr3:51911345-51911346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369503502	chr3:51911399-51911400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51905600-51911400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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