| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:59595903-59596180 | Common:5; Rare:69 | ||||
| chr12:62260040-62260452 | Common:1; Rare:154 | ||||
| chr12:63779729-63779921 | Common:2; Rare:71; Clinvar (benign):1 | ||||
| chr12:63844711-63844828 | Common:1; Rare:33 | ||||
| chr12:64222233-64222349 | Rare:43 | ||||
| chr12:64404268-64404639 | Common:5; Rare:136 | ||||
| chr12:64452034-64452174 | Common:1; Rare:51 | ||||
| chr12:64610310-64610599 | Common:3; Rare:105 | ||||
| chr12:64759364-64759496 | Common:1; Rare:43; Clinvar:3 | ||||
| chr12:65169380-65169624 | Common:1; Rare:83; Clinvar:2 | ||||
| chr12:65824808-65824854 | Rare:11 | ||||
| chr12:65824944-65825114 | Rare:40 | ||||
| chr12:66130703-66130887 | Rare:58 | ||||
| chr12:67269141-67269421 | Common:2; Rare:83 | ||||
| chr12:67269524-67269762 | Common:1; Rare:74 |