| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:14770703-14770718 | Rare:6 | ||||
| chr12:14770976-14771266 | Common:2; Rare:140 | ||||
| chr12:14774184-14774698 | Common:3; Rare:162 | ||||
| chr12:14802937-14803087 | Common:3; Rare:36 | ||||
| chr12:14803403-14803768 | Common:2; Rare:103 | ||||
| chr12:14884217-14884523 | Common:3; Rare:60; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:14929111-14929198 | Common:1; Rare:28 | ||||
| chr12:15882232-15882783 | Common:1; Rare:189 | ||||
| chr12:15911188-15911400 | Common:5; Rare:79 | ||||
| chr12:19129560-19129802 | Common:1; Rare:125 | ||||
| chr12:19236833-19237270 | Rare:81 | ||||
| chr12:19439312-19439697 | Common:3; Rare:140 | ||||
| chr12:20369533-20369908 | Common:3; Rare:168 | ||||
| chr12:20571944-20572129 | Common:3; Rare:25 | ||||
| chr12:21437592-21437907 | Common:6; Rare:147 |