| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38906634-38907071 | Common:2; Rare:89 | ||||
| chr12:39442432-39442480 | Rare:13 | ||||
| chr12:39442599-39442922 | Common:1; Rare:70 | ||||
| chr12:39443023-39443402 | Common:2; Rare:106; Clinvar:8; Clinvar (benign):5 | ||||
| chr12:39443556-39443640 | Rare:14 | ||||
| chr12:39619515-39619613 | Common:1; Rare:28 | ||||
| chr12:39619702-39619881 | Common:1; Rare:27 | ||||
| chr12:39619897-39620331 | Common:1; Rare:79 | ||||
| chr12:40105453-40105672 | Common:2; Rare:73 | ||||
| chr12:40105953-40106243 | Common:1; Rare:108 | ||||
| chr12:40224575-40224731 | Common:1; Rare:43 | ||||
| chr12:40224781-40225162 | Common:5; Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:40225245-40225428 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr12:40225648-40225691 | Rare:13 | ||||
| chr12:42144553-42144700 | Common:6; Rare:79 |