Variant report
| Variant | rs73087638 |
|---|---|
| Chromosome Location | chr12:44400391-44400392 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:44361400-44401400 | Weak transcription | Aorta | Aorta |
| 2 | chr12:44383200-44402400 | Weak transcription | HSMMtube | muscle |
| 3 | chr12:44390800-44439200 | Weak transcription | Esophagus | oesophagus |
| 4 | chr12:44394600-44403200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 5 | chr12:44394800-44401800 | Weak transcription | HMEC | breast |
| 6 | chr12:44395000-44401400 | Weak transcription | Fetal Intestine Large | intestine |
| 7 | chr12:44398000-44402400 | Weak transcription | HSMM | muscle |
| 8 | chr12:44399200-44401800 | Weak transcription | Duodenum Mucosa | Duodenum |
| 9 | chr12:44399400-44401000 | Strong transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 10 | chr12:44400200-44401400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 11 | chr12:44400200-44401800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
