| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62278045-62278445 | Common:1; Rare:90 | ||||
| chr12:62466022-62466439 | Rare:163 | ||||
| chr12:62466593-62466920 | Rare:318 | ||||
| chr12:62466823-62467223 | Common:2; Rare:86 | ||||
| chr12:62467237-62467348 | Common:1; Rare:30 | ||||
| chr12:62467559-62467959 | Common:1; Rare:62 | ||||
| chr12:62933240-62933645 | Common:4; Rare:155 | ||||
| chr12:62933897-62934860 | Common:4; Rare:433 | ||||
| chr12:62935039-62935439 | Common:6; Rare:284 | ||||
| chr12:63779599-63779999 | Common:15; Rare:464; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:63779983-63780893 | Common:2; Rare:461; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):8 | ||||
| chr12:63843560-63843900 | Common:5; Rare:98 | ||||
| chr12:63843920-63844152 | Common:6; Rare:97 | ||||
| chr12:64221540-64222070 | Rare:161 | ||||
| chr12:64222116-64222801 | Common:5; Rare:362 |