| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108598009-108598428 | Common:2; Rare:92 | ||||
| chr12:108731480-108731686 | Common:2; Rare:76 | ||||
| chr12:108826396-108826750 | Common:1; Rare:78 | ||||
| chr12:108827045-108827370 | Common:3; Rare:79 | ||||
| chr12:109052509-109052660 | Common:2; Rare:48 | ||||
| chr12:109477260-109477643 | Common:3; Rare:100 | ||||
| chr12:109519265-109519586 | Common:1; Rare:65 | ||||
| chr12:109573435-109573852 | Common:3; Rare:136; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880344-109880658 | Common:1; Rare:97 | ||||
| chr12:109996309-109996439 | Common:2; Rare:35 | ||||
| chr12:110124128-110124441 | Common:2; Rare:104 | ||||
| chr12:110281012-110281222 | Rare:77 | ||||
| chr12:110468673-110468909 | Rare:58 | ||||
| chr12:110502058-110502231 | Common:1; Rare:63 | ||||
| chr12:111685767-111686105 | Rare:127 |