Variant report
| Variant | rs1798020 |
|---|---|
| Chromosome Location | chr12:44739393-44739394 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:44699000-44782000 | Weak transcription | Aorta | Aorta |
| 2 | chr12:44709200-44743200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 3 | chr12:44712400-44765800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 4 | chr12:44728400-44744800 | Weak transcription | Esophagus | oesophagus |
| 5 | chr12:44736400-44740400 | Weak transcription | Fetal Intestine Small | intestine |
| 6 | chr12:44736800-44742800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
