Variant report
| Variant | esv3368942 |
|---|---|
| Chromosome Location | chr19:24160893-24161090 |
| 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 | rs139477559 | chr19:24160914-24160915 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs577302253 | chr19:24160932-24160933 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 3 | rs538980234 | chr19:24160943-24160944 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 4 | rs557269691 | chr19:24160961-24160962 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 5 | rs149895342 | chr19:24160991-24160992 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 6 | rs542772807 | chr19:24160992-24160993 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 7 | rs571633861 | chr19:24161002-24161003 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 8 | rs572847057 | chr19:24161018-24161019 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 9 | rs10423626 | chr19:24161031-24161032 | ZNF genes & repeats Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
| 10 | rs144938027 | chr19:24161034-24161035 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 11 | rs189112733 | chr19:24161036-24161037 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 12 | rs7508552 | chr19:24161045-24161046 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 13 | rs562810720 | chr19:24161046-24161047 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 14 | rs7508554 | chr19:24161057-24161058 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
| 15 | rs530256435 | chr19:24161063-24161064 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:40)
| Disease | PMID | Source |
|---|---|---|
| Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
| Prostate cancer | 16573809 | CNVD |
| Chordoma | 18071362 | CNVD |
| Metanephric adenoma | 20802469 | CNVD |
| Ewing''s sarcoma | 21437220 | CNVD |
| Glioblastoma multiforme | 21080181 | CNVD |
| Medulloblastoma | 21979893 | CNVD |
| Oligodendroglial tumors | 17285580 | CNVD |
| Oral cancer | 21386901 | CNVD |
| ovarian endometriomas | 16273235 | CNVD |
| Endometrial cancer | 22040021 | CNVD |
| Acute myeloid leukemia | 16864856 | CNVD |
| Breast cancer | 21264507 | CNVD |
| Esophageal squamous carcinoma | 21637470 | CNVD |
| Glioblastoma multiforme | 17387387 | CNVD |
| Cervical cancer | 21063398 | CNVD |
| Myelodysplastic syndrome | 17634407 | CNVD |
| Acute lymphoblastic leukemia | 22237106 | CNVD |
| Chordoma | 21602918 | CNVD |
| Chronic lymphocytic leukemia | 21546498 | CNVD |
| Cancer | 21637783 | CNVD |
| Retinoblastoma | 21504564 | CNVD |
| Ovarian cancer | 21720365 | CNVD |
| Cancer | 20164919 | CNVD |
| Thoracic aortic aneurysm | 21092924 | CNVD |
| T-cell prolymphocytic leukemia | 19278963 | CNVD |
| Prostate cancer | 18632612 | CNVD |
| Autism | 22495311 | CNVD |
| Acute lymphoblastic leukemia | 20435627 | CNVD |
| Acute lymphoblastic leukemia | 21248843 | CNVD |
| Lung cancer | 18438408 | CNVD |
| Adenoid cystic carcinoma | 18698036 | CNVD |
| Myelofibrosis | 22110671 | CNVD |
| Cancer | 21183584 | CNVD |
| Colorectal cancer | 20459617 | CNVD |
| Ductal carcinoma | 22052326 | CNVD |
| Cancer | 20164920 | CNVD |
| small cell lung cancer | 20016488 | CNVD |
| Renal cell carcinoma | 18194544 | CNVD |
| Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr19:24160200-24161200 | Enhancers | Placenta | Placenta |
| 2 | chr19:24160800-24161400 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
