Variant report
| Variant | rs369259099 |
|---|---|
| Chromosome Location | chr12:44318605-44318606 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:44307400-44324000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 2 | chr12:44311400-44324600 | Weak transcription | Left Ventricle | heart |
| 3 | chr12:44315200-44324200 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 4 | chr12:44316000-44321200 | Weak transcription | HSMMtube | muscle |
| 5 | chr12:44317400-44321200 | Weak transcription | Fetal Intestine Large | intestine |
| 6 | chr12:44317600-44321400 | Weak transcription | Fetal Intestine Small | intestine |
| 7 | chr12:44317600-44325400 | Weak transcription | Rectal Smooth Muscle | rectum |
| 8 | chr12:44317800-44321600 | Weak transcription | Fetal Stomach | stomach |
| 9 | chr12:44318400-44319600 | Strong transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 10 | chr12:44318600-44318800 | Enhancers | H1 Cell Line | embryonic stem cell |
| 11 | chr12:44318600-44319000 | ZNF genes & repeats | Esophagus | oesophagus |
