| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31959269-31959468 | Common:2; Rare:63 | ||||
| chr12:32399243-32399577 | Common:4; Rare:90 | ||||
| chr12:32399794-32399953 | Common:1; Rare:48 | ||||
| chr12:32755884-32756021 | Rare:44 | ||||
| chr12:32896764-32897011 | Common:3; Rare:82; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:38905499-38905773 | Common:4; Rare:77 | ||||
| chr12:42325989-42326229 | Common:2; Rare:78 | ||||
| chr12:43758749-43759016 | Common:2; Rare:75; Clinvar:2 | ||||
| chr12:43806083-43806434 | Common:4; Rare:132 | ||||
| chr12:45215992-45216184 | Rare:63 | ||||
| chr12:45922530-45922685 | Rare:31 | ||||
| chr12:45990474-45990917 | Common:2; Rare:143 | ||||
| chr12:46267340-46267472 | Rare:25 | ||||
| chr12:46268616-46268669 | Rare:13 | ||||
| chr12:46362296-46362635 | Common:2; Rare:91 |