Variant report
| Variant | rs55684676 |
|---|---|
| Chromosome Location | chr2:191415141-191415142 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:191403000-191416800 | Weak transcription | Gastric | stomach |
| 2 | chr2:191405400-191416800 | Weak transcription | Esophagus | oesophagus |
| 3 | chr2:191410800-191418200 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
| 4 | chr2:191411000-191443000 | Weak transcription | Right Atrium | heart |
| 5 | chr2:191411800-191416800 | Weak transcription | Psoas Muscle | Psoas |
| 6 | chr2:191412000-191416600 | Weak transcription | HepG2 | liver |
| 7 | chr2:191413000-191416000 | Weak transcription | Primary T cells from cord blood | blood |
| 8 | chr2:191413600-191416600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
