| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93571416-93571715 | Common:1; Rare:80 | ||||
| chr12:93571757-93571854 | Common:5; Rare:35 | ||||
| chr12:93677236-93677539 | Rare:67 | ||||
| chr12:93677550-93677735 | Rare:53 | ||||
| chr12:93677886-93677972 | Common:1; Rare:13 | ||||
| chr12:94262268-94262648 | Common:2; Rare:87 | ||||
| chr12:94459616-94460150 | Common:8; Rare:144 | ||||
| chr12:94460241-94460321 | Common:1; Rare:10 | ||||
| chr12:94460394-94460499 | Rare:29 | ||||
| chr12:95003391-95003469 | Rare:12 | ||||
| chr12:95003596-95003862 | Common:3; Rare:109; Clinvar (benign):6 | ||||
| chr12:95072894-95072975 | Common:1; Rare:22 | ||||
| chr12:95073579-95073722 | Rare:40 | ||||
| chr12:95217271-95217977 | Common:6; Rare:185 | ||||
| chr12:95218000-95218085 | Common:1; Rare:11 |