| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110582482-110582557 | Rare:20 | ||||
| chr12:110590921-110591119 | Common:1; Rare:30 | ||||
| chr12:110605692-110605911 | Common:1; Rare:29 | ||||
| chr12:110605930-110606121 | Rare:22 | ||||
| chr12:110634483-110634721 | Rare:55; Clinvar (benign):1 | ||||
| chr12:110661384-110661529 | Rare:44 | ||||
| chr12:110661640-110661956 | Common:3; Rare:60 | ||||
| chr12:110667808-110668021 | Rare:28 | ||||
| chr12:110668636-110668699 | Rare:6 | ||||
| chr12:110669193-110669304 | Rare:21 | ||||
| chr12:110669689-110669805 | Rare:22 | ||||
| chr12:110670191-110670451 | Common:1; Rare:38 | ||||
| chr12:110677287-110677590 | Common:2; Rare:52 | ||||
| chr12:110677829-110677913 | Rare:18 | ||||
| chr12:110686385-110686590 | Common:1; Rare:39 |