Variant report
| Variant | esv3448999 |
|---|---|
| Chromosome Location | chr12:40105334-40105735 |
| allele | n/a |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
| No data |
| No data |
| No data |
| No data |
| No data |
Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs12312036 | chr12:40105337-40105338 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs148281565 | chr12:40105340-40105341 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs111219585 | chr12:40105341-40105342 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs116223090 | chr12:40105343-40105344 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs565455545 | chr12:40105345-40105346 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs115236213 | chr12:40105352-40105353 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs202048510 | chr12:40105368-40105369 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs550957151 | chr12:40105370-40105371 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs117878903 | chr12:40105371-40105372 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 10 | rs150684932 | chr12:40105374-40105375 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs145266103 | chr12:40105375-40105376 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs111203744 | chr12:40105376-40105377 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs372918985 | chr12:40105392-40105393 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs12818191 | chr12:40105395-40105396 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 15 | rs201675618 | chr12:40105400-40105401 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:56)
| Disease | PMID | Source |
|---|---|---|
| Chronic lymphocytic leukemia | 21546498 | CNVD |
| Seminomas | 18059402 | CNVD |
| Wilms tumour | 21544195 | CNVD |
| Esophageal cancer | 21851588 | CNVD |
| Lung cancer | 20668451 | CNVD |
| Breast cancer | 20668451 | CNVD |
| Cancer | 20668451 | CNVD |
| Ovarian cancer | 20668451 | CNVD |
| Pancreas cancer | 20668451 | CNVD |
| Prostate cancer | 20668451 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Testicular germ cell tumor | 18059402 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Malaria | 21533027 | CNVD |
| Chronic lymphocytic leukemia | 22228453 | CNVD |
| Basal cell lymphoma | 17053054 | CNVD |
| Chronic lymphocytic leukemia | 21670202 | CNVD |
| Ewing''s sarcoma | 17952124 | CNVD |
| Acute lymphoblastic leukemia | 20435627 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| Autism | 22495311 | CNVD |
| Cancer | 20164919 | CNVD |
| Neurodevelopmental disorder | 22521361 | CNVD |
| Acute lymphoblastic leukemia | 21390130 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| T-cell prolymphocytic leukemia | 17713554 | CNVD |
| Renal cell carcinoma | 18194544 | CNVD |
| Breast cancer | 21949216 | CNVD |
| Carcinoma ex pleomorphic adenoma | 18828159 | CNVD |
| Acute myeloid leukemia | 16864856 | CNVD |
| Cancer | 21637783 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Renal cell carcinoma | 19461508 | CNVD |
| Burkitt''s lymphoma | 18698080 | CNVD |
| Astrocytoma | 17387387 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Glioblastoma multiforme | 19960244 | CNVD |
| Gastrointestinal stromal cancer | 20470368 | CNVD |
| Adenoid cystic carcinoma | 17372589 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Breast cancer | 17603634 | CNVD |
| Cancer | 21183584 | CNVD |
| Hirschsprung''s Disease | 21712996 | CNVD |
| Lissencephaly | 21572526 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Acute myeloid leukemia | 21251322 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Autism | 20858243 | CNVD |
| Malignant peripheral nerve sheath tumor | 18522746 | CNVD |
| Adenoid cystic carcinoma | 18698036 | CNVD |
| Breast cancer | 19602461 | CNVD |
| Breast cancer | 17899364 | CNVD |
| Cancer | 20164920 | CNVD |
| Colorectal cancer | 16272173 | CNVD |
| Breast cancer | 22522925 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:40104000-40105400 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
