| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57455036-57455335 | Rare:54 | ||||
| chr12:57459889-57459893 | Rare:1 | ||||
| chr12:57488798-57489109 | Common:3; Rare:72; Clinvar (benign):2 | ||||
| chr12:57520444-57520708 | Common:2; Rare:82 | ||||
| chr12:57716462-57716724 | Rare:71 | ||||
| chr12:57772087-57772251 | Rare:56 | ||||
| chr12:57846926-57847221 | Common:2; Rare:109 | ||||
| chr12:58920460-58920653 | Common:2; Rare:64 | ||||
| chr12:62260165-62260496 | Common:1; Rare:123 | ||||
| chr12:64759341-64759511 | Common:1; Rare:56; Clinvar:3 | ||||
| chr12:65824454-65824503 | Rare:6 | ||||
| chr12:65824872-65825141 | Common:1; Rare:66 | ||||
| chr12:66130700-66130861 | Rare:57 | ||||
| chr12:67269257-67269441 | Common:1; Rare:62 | ||||
| chr12:68316865-68316891 | Rare:2 |