| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53181306-53181449 | Rare:33 | ||||
| chr12:53232141-53232451 | Common:2; Rare:66 | ||||
| chr12:53252049-53252217 | Common:3; Rare:63 | ||||
| chr12:53321232-53321423 | Common:1; Rare:69; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:53380106-53380282 | Common:3; Rare:74 | ||||
| chr12:53467038-53467336 | Rare:79 | ||||
| chr12:53492960-53493251 | Common:4; Rare:75 | ||||
| chr12:53500167-53500256 | Rare:14 | ||||
| chr12:53500663-53500929 | Common:3; Rare:62 | ||||
| chr12:53501213-53501357 | Rare:35 | ||||
| chr12:53501524-53501597 | Rare:16 | ||||
| chr12:53625920-53626178 | Common:1; Rare:69 | ||||
| chr12:53676027-53676416 | Common:3; Rare:178 | ||||
| chr12:53727403-53727713 | Rare:66 | ||||
| chr12:54053553-54053863 | Rare:50 |