| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64404178-64404713 | Common:6; Rare:184 | ||||
| chr12:64452041-64452175 | Common:1; Rare:49 | ||||
| chr12:64759104-64759324 | Rare:68; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:64759330-64759479 | Rare:50; Clinvar:3 | ||||
| chr12:66130719-66130861 | Rare:47 | ||||
| chr12:66169937-66170065 | Common:1; Rare:37 | ||||
| chr12:67269541-67269665 | Rare:40 | ||||
| chr12:68332265-68332588 | Common:1; Rare:103 | ||||
| chr12:68610695-68611048 | Common:1; Rare:148 | ||||
| chr12:68686794-68687062 | Common:5; Rare:85 | ||||
| chr12:68807905-68808249 | Common:4; Rare:105 | ||||
| chr12:68808472-68808480 | Rare:2 | ||||
| chr12:68808694-68809027 | Common:3; Rare:68; Clinvar:1 | ||||
| chr12:68933109-68933350 | Rare:79 | ||||
| chr12:69239459-69239678 | Common:2; Rare:89 |