| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48814683-48814862 | Rare:31 | ||||
| chr12:48815460-48815593 | Common:1; Rare:33 | ||||
| chr12:48839848-48840092 | Rare:62 | ||||
| chr12:48852086-48852390 | Common:2; Rare:86 | ||||
| chr12:49002893-49003192 | Common:1; Rare:74 | ||||
| chr12:49018736-49018933 | Common:1; Rare:83 | ||||
| chr12:49131296-49131642 | Common:2; Rare:135 | ||||
| chr12:49188488-49188651 | Common:2; Rare:21 | ||||
| chr12:49188981-49189222 | Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264775-49265155 | Common:4; Rare:141 | ||||
| chr12:49322986-49323277 | Common:2; Rare:64 | ||||
| chr12:49367226-49367562 | Common:1; Rare:90 | ||||
| chr12:49568089-49568197 | Common:2; Rare:41 | ||||
| chr12:49623279-49623572 | Common:1; Rare:83 | ||||
| chr12:49750505-49750673 | Rare:29 |