| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:681661-682074 | Common:5; Rare:111 | ||||
| chr12:682470-682900 | Common:5; Rare:125 | ||||
| chr12:685460-685690 | Common:3; Rare:81 | ||||
| chr12:719056-719456 | Common:6; Rare:122 | ||||
| chr12:719451-720090 | Common:4; Rare:369 | ||||
| chr12:720244-720715 | Common:7; Rare:85 | ||||
| chr12:722440-722790 | Common:4; Rare:121 | ||||
| chr12:751116-751905 | Common:5; Rare:397 | ||||
| chr12:751836-751995 | Common:1; Rare:25 | ||||
| chr12:753766-754534 | Common:15; Rare:380; Clinvar:17; Clinvar (benign):19 | ||||
| chr12:754919-755319 | Common:2; Rare:88 | ||||
| chr12:795451-795570 | Rare:17 | ||||
| chr12:800509-800647 | Common:2; Rare:32 | ||||
| chr12:800631-801564 | Common:3; Rare:233 | ||||
| chr12:818289-818867 | Common:7; Rare:149 |