| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57455926-57455992 | Common:1; Rare:12 | ||||
| chr12:57459968-57460008 | Rare:8 | ||||
| chr12:57487809-57488163 | Common:1; Rare:91; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:57488293-57488379 | Common:1; Rare:20 | ||||
| chr12:57488716-57488743 | Rare:3 | ||||
| chr12:57520413-57520854 | Common:4; Rare:126 | ||||
| chr12:57520897-57521009 | Rare:25 | ||||
| chr12:57522418-57522908 | Common:3; Rare:172 | ||||
| chr12:57523148-57523277 | Rare:31 | ||||
| chr12:57547115-57547427 | Common:1; Rare:62 | ||||
| chr12:57549945-57550086 | Rare:37 | ||||
| chr12:57591031-57591285 | Common:6; Rare:116 | ||||
| chr12:57604554-57604648 | Rare:14 | ||||
| chr12:57604735-57604865 | Rare:27 | ||||
| chr12:57605004-57605116 | Rare:18 |