| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56130792-56131080 | Rare:87 | ||||
| chr12:56131257-56131562 | Common:1; Rare:74 | ||||
| chr12:56142831-56143292 | Rare:135 | ||||
| chr12:56152481-56152629 | Rare:45 | ||||
| chr12:56181492-56181776 | Rare:72 | ||||
| chr12:56189435-56189834 | Common:1; Rare:117 | ||||
| chr12:56221856-56222086 | Common:1; Rare:58 | ||||
| chr12:56258300-56258413 | Common:1; Rare:36 | ||||
| chr12:56299964-56300166 | Common:2; Rare:74 | ||||
| chr12:56300246-56300530 | Common:1; Rare:84 | ||||
| chr12:56315821-56316205 | Common:2; Rare:99 | ||||
| chr12:56333872-56334189 | Common:1; Rare:90 | ||||
| chr12:56338574-56338907 | Rare:50 | ||||
| chr12:56354216-56354501 | Rare:52; Clinvar (benign):1 | ||||
| chr12:56360258-56360575 | Common:1; Rare:72 |