| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56645956-56646251 | Common:1; Rare:67 | ||||
| chr12:56688103-56688595 | Common:5; Rare:169 | ||||
| chr12:56724450-56724695 | Common:3; Rare:60 | ||||
| chr12:56752306-56752380 | Rare:25 | ||||
| chr12:57087837-57087952 | Common:1; Rare:32 | ||||
| chr12:57111333-57111441 | Rare:26 | ||||
| chr12:57111833-57111913 | Common:1; Rare:16 | ||||
| chr12:57229572-57229771 | Common:3; Rare:87 | ||||
| chr12:57229996-57230212 | Rare:46 | ||||
| chr12:57240366-57240653 | Rare:57 | ||||
| chr12:57477791-57478115 | Rare:74 | ||||
| chr12:57488775-57489101 | Common:3; Rare:74; Clinvar (benign):2 | ||||
| chr12:57520453-57520720 | Common:2; Rare:82 | ||||
| chr12:57522570-57522895 | Common:3; Rare:124 | ||||
| chr12:57591108-57591280 | Common:4; Rare:79 |