| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110469125-110469385 | Common:1; Rare:48 | ||||
| chr12:110501890-110502357 | Common:1; Rare:181 | ||||
| chr12:110546383-110546671 | Rare:27 | ||||
| chr12:110582732-110582972 | Common:3; Rare:70 | ||||
| chr12:110583221-110583546 | Rare:91 | ||||
| chr12:110613921-110614213 | Rare:88; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110689096-110689124 | Rare:6 | ||||
| chr12:110742253-110742465 | Common:3; Rare:62 | ||||
| chr12:110742829-110743269 | Common:3; Rare:148 | ||||
| chr12:110847033-110847172 | Common:1; Rare:35 | ||||
| chr12:111033441-111033779 | Rare:74 | ||||
| chr12:111034394-111034623 | Rare:49 | ||||
| chr12:111369037-111369272 | Common:1; Rare:65 | ||||
| chr12:111405344-111406165 | Common:2; Rare:217 | ||||
| chr12:111434600-111434919 | Common:2; Rare:59 |