Variant report
| Variant | rs1798032 |
|---|---|
| Chromosome Location | chr12:44765318-44765319 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:44699000-44782000 | Weak transcription | Aorta | Aorta |
| 2 | chr12:44712400-44765800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 3 | chr12:44754000-44775600 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 4 | chr12:44760200-44770400 | Weak transcription | Left Ventricle | heart |
| 5 | chr12:44760800-44769600 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 6 | chr12:44762000-44777400 | Weak transcription | Fetal Intestine Small | intestine |
| 7 | chr12:44762000-44791200 | Weak transcription | Fetal Intestine Large | intestine |
| 8 | chr12:44764000-44769000 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
| 9 | chr12:44764600-44770600 | Weak transcription | Placenta Amnion | Placenta Amnion |
