| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109477006-109477734 | Common:5; Rare:182 | ||||
| chr12:109573066-109573317 | Common:3; Rare:53 | ||||
| chr12:109573432-109573883 | Common:3; Rare:147; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr12:109713950-109713985 | Rare:9 | ||||
| chr12:109880366-109880739 | Common:2; Rare:107 | ||||
| chr12:109900111-109900696 | Rare:145 | ||||
| chr12:109900893-109901193 | Common:1; Rare:66 | ||||
| chr12:109996296-109996469 | Common:2; Rare:51 | ||||
| chr12:109999039-109999510 | Rare:107 | ||||
| chr12:109999554-109999654 | Rare:18 | ||||
| chr12:110048306-110048790 | Common:2; Rare:126 | ||||
| chr12:110124122-110124630 | Common:2; Rare:136 | ||||
| chr12:110124718-110124808 | Rare:14 | ||||
| chr12:110124819-110124885 | Rare:6 | ||||
| chr12:110280487-110280730 | Rare:58 |