| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6235225-6235574 | Common:1; Rare:104 | ||||
| chr12:6295087-6295397 | Rare:53 | ||||
| chr12:6339329-6339494 | Rare:30 | ||||
| chr12:6372566-6372756 | Rare:30 | ||||
| chr12:6526311-6526584 | Common:1; Rare:74; Clinvar:1 | ||||
| chr12:6537739-6538220 | Common:3; Rare:177 | ||||
| chr12:6770153-6770675 | Rare:137 | ||||
| chr12:6927585-6927738 | Rare:44 | ||||
| chr12:6933833-6934576 | Common:1; Rare:196 | ||||
| chr12:6962543-6962618 | Common:1; Rare:12 | ||||
| chr12:6963049-6963240 | Common:1; Rare:36 | ||||
| chr12:6974223-6974403 | Rare:51 | ||||
| chr12:7088608-7088839 | Common:1; Rare:72; Clinvar (pathogenic):1 | ||||
| chr12:7089293-7089734 | Common:3; Rare:143 | ||||
| chr12:7103007-7103307 | Common:2; Rare:45 |