Variant report
| Variant | esv3424909 |
|---|---|
| Chromosome Location | chr12:59689499-59689836 |
| 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:19 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs578097053 | chr12:59689557-59689558 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs545365326 | chr12:59689563-59689564 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs558642321 | chr12:59689589-59689590 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs560235197 | chr12:59689593-59689594 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs564590580 | chr12:59689607-59689608 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs142476916 | chr12:59689615-59689616 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs542470259 | chr12:59689617-59689618 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs376237475 | chr12:59689641-59689642 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs36094921 | chr12:59689652-59689653 | Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 10 | rs535842451 | chr12:59689663-59689664 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs549429990 | chr12:59689686-59689687 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs35722619 | chr12:59689705-59689706 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs564620775 | chr12:59689720-59689721 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs532005148 | chr12:59689721-59689722 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 15 | rs547363404 | chr12:59689723-59689724 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 16 | rs187269014 | chr12:59689733-59689734 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 17 | rs36071173 | chr12:59689739-59689740 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 18 | rs534465406 | chr12:59689787-59689788 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 19 | rs188172523 | chr12:59689798-59689799 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:82)
| Disease | PMID | Source |
|---|---|---|
| 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 |
| Chronic lymphocytic leukemia | 21546498 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Malaria | 21533027 | CNVD |
| Chronic lymphocytic leukemia | 22228453 | CNVD |
| Basal cell lymphoma | 17053054 | CNVD |
| Chronic lymphocytic leukemia | 21670202 | CNVD |
| Acute lymphoblastic leukemia | 20435627 | CNVD |
| Hodgkin''s lymphoma | 17606441 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| Autism | 22495311 | CNVD |
| Neurodevelopmental disorder | 22521361 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | 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 |
| Lissencephaly | 21572526 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Breast cancer | 19602461 | CNVD |
| Breast cancer | 17899364 | CNVD |
| Colorectal cancer | 16272173 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Metanephric adenoma | 20802469 | CNVD |
| Glioblastoma multiforme | 17387387 | CNVD |
| liposarcomas | 17372913 | CNVD |
| Non-small cell lung cancer | 24170126 | CNVD |
| Cancer | 16751803 | CNVD |
| Endometrioid adenocarcinoma | 16974079 | CNVD |
| Breast cancer | 21785460 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| low-grade B-cell lymphoma tumor | 18367492 | CNVD |
| Hodgkin''s lymphoma | 18179710 | CNVD |
| Urothelial cell carcinoma | 18451213 | CNVD |
| Melanoma | 18172304 | CNVD |
| Glioblastoma multiforme | 21390271 | CNVD |
| Cancer | 20164919 | CNVD |
| Leukemia | 18628472 | CNVD |
| Glioblastoma multiforme | 22291905 | CNVD |
| Glioblastoma multiforme | 19435819 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Phyllodes tumor | 17334353 | CNVD |
| Glaucoma | 21310917 | CNVD |
| Breast cancer | 16272173 | CNVD |
| Mental retardation | 19951919 | CNVD |
| Glaucoma | 21447600 | CNVD |
| Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
| Developmental delay | 21267005 | CNVD |
| 12q14 microdeletion syndrome | 21267005 | CNVD |
| Developmental delay | 19277063 | CNVD |
| Dwarfism | 19277063 | CNVD |
| Fibroblasts | 20926602 | CNVD |
| Follicular lymphoma | 18703704 | CNVD |
| Acute myeloid leukemia | 21251322 | CNVD |
| Glioblastoma multiforme | 20080666 | CNVD |
| Medulloblastoma | 19270706 | CNVD |
| Breast cancer | 17133270 | CNVD |
| Malignant peripheral nerve sheath tumor | 18522746 | CNVD |
| Gastrointestinal stromal cancer | 20877625 | CNVD |
| Glioblastoma | 17090523 | CNVD |
| Multiple myeloma | 16616336 | CNVD |
| Lung cancer | 16773561 | CNVD |
| Primary mediastinal b-cell lymphoma | 17728785 | CNVD |
| Breast cancer | 21364760 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:59687000-59692200 | Weak transcription | Gastric | stomach |
