| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108561110-108561500 | Common:7; Rare:186 | ||||
| chr12:108562390-108562637 | Common:5; Rare:170; Clinvar:1 | ||||
| chr12:108731453-108731830 | Common:3; Rare:120 | ||||
| chr12:108731890-108732300 | Common:6; Rare:196 | ||||
| chr12:108857571-108857813 | Common:2; Rare:215 | ||||
| chr12:109052470-109052659 | Common:3; Rare:55 | ||||
| chr12:109097450-109097680 | Rare:147; Clinvar:4 | ||||
| chr12:109097863-109098239 | Common:10; Rare:206 | ||||
| chr12:109115840-109116100 | Common:1; Rare:38 | ||||
| chr12:109116120-109116510 | Common:10; Rare:130 | ||||
| chr12:109154541-109154745 | Common:1; Rare:56 | ||||
| chr12:109477284-109477679 | Common:6; Rare:197 | ||||
| chr12:109573408-109573876 | Common:10; Rare:319; Clinvar:18; Clinvar (benign):16; Clinvar (pathogenic):4 | ||||
| chr12:109880381-109880571 | Common:1; Rare:74 | ||||
| chr12:109900196-109900365 | Rare:127 |