Variant report
| Variant | esv1651252 |
|---|---|
| Chromosome Location | chr9:141031612-141031624 |
| 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:2 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | rs71495314 | chr9:141031613-141031614 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
| 2 | rs60175300 | chr9:141031619-141031620 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Variant related diseases (count:19)
| Disease | PMID | Source |
|---|---|---|
| Leukemia | 17361228 | CNVD |
| Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
| Glioblastoma | 16823260 | CNVD |
| Oral squamous cell carcinoma | 17134496 | CNVD |
| Cardiac fibroma | 18329553 | CNVD |
| Lung cancer | 19147751 | CNVD |
| Cervical cancer | 17311676 | CNVD |
| Endometrioid adenocarcinoma | 16974079 | CNVD |
| Gastric cancer | 17908304 | CNVD |
| Adenoid cystic carcinoma | 18698036 | CNVD |
| Salivary gland adenoid cystic carcinoma | 17545515 | CNVD |
| Chordoma | 18071362 | CNVD |
| Primary mediastinal b-cell lymphoma | 17728785 | CNVD |
| Sudden cardiac death | 19188705 | CNVD |
| Myoepithelioma | 18604193 | CNVD |
| Tuberous sclerosis | 19566914 | CNVD |
| Multiple myeloma | 16616336 | CNVD |
| Acute lymphoblastic leukemia | 19100363 | CNVD |
| Mantle cell lymphoma | 19029149 | CNVD |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:140988200-141044600 | Weak transcription | Right Atrium | heart |
