Variant report
| Variant | rs11836418 |
|---|---|
| Chromosome Location | chr12:57328328-57328329 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:57321400-57328400 | Enhancers | Fetal Thymus | thymus |
| 2 | chr12:57322000-57328800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 3 | chr12:57325400-57329400 | Enhancers | Placenta | Placenta |
| 4 | chr12:57325800-57335200 | Weak transcription | Fetal Intestine Large | intestine |
| 5 | chr12:57326400-57328800 | Weak transcription | A549 | lung |
| 6 | chr12:57326400-57335200 | Weak transcription | Placenta Amnion | Placenta Amnion |
| 7 | chr12:57327000-57335200 | Weak transcription | Spleen | Spleen |
| 8 | chr12:57327200-57328400 | Enhancers | Monocytes-CD14+_RO01746 | blood |
| 9 | chr12:57327200-57328600 | Weak transcription | HMEC | breast |
| 10 | chr12:57327200-57328600 | Weak transcription | NHEK | skin |
| 11 | chr12:57327200-57329000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 12 | chr12:57327400-57330200 | Enhancers | Esophagus | oesophagus |
| 13 | chr12:57327600-57329600 | Weak transcription | K562 | blood |
| 14 | chr12:57328000-57330000 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 15 | chr12:57328000-57330200 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 16 | chr12:57328200-57335000 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
