| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109573097-109573300 | Common:2; Rare:42 | ||||
| chr12:109573427-109573808 | Common:3; Rare:127; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109713593-109713848 | Common:1; Rare:78 | ||||
| chr12:109880318-109880759 | Common:2; Rare:127 | ||||
| chr12:109900126-109900722 | Common:1; Rare:149 | ||||
| chr12:109996180-109996445 | Common:2; Rare:75 | ||||
| chr12:109998863-109999479 | Rare:126 | ||||
| chr12:110048426-110048792 | Common:2; Rare:89 | ||||
| chr12:110049152-110049297 | Common:1; Rare:30 | ||||
| chr12:110049772-110050039 | Common:1; Rare:56 | ||||
| chr12:110124108-110124474 | Common:2; Rare:115 | ||||
| chr12:110280789-110280851 | Rare:18 | ||||
| chr12:110280888-110281352 | Common:1; Rare:167; Clinvar (benign):1 | ||||
| chr12:110403592-110403766 | Common:2; Rare:92 | ||||
| chr12:110404096-110404176 | Common:2; Rare:19 |