Variant report
| Variant | rs840765 |
|---|---|
| Chromosome Location | chr12:44703597-44703598 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:44694600-44706000 | Weak transcription | Fetal Muscle Trunk | muscle |
| 2 | chr12:44699000-44712600 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 3 | chr12:44699000-44713800 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
| 4 | chr12:44699000-44736000 | Weak transcription | Pancreas | Pancrea |
| 5 | chr12:44699000-44782000 | Weak transcription | Aorta | Aorta |
| 6 | chr12:44700000-44705800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 7 | chr12:44701000-44704200 | Weak transcription | Fetal Brain Male | brain |
| 8 | chr12:44703200-44707600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 9 | chr12:44703400-44711800 | Weak transcription | Fetal Intestine Small | intestine |
