| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48716668-48717008 | Common:4; Rare:102 | ||||
| chr12:48814336-48814496 | Common:1; Rare:33 | ||||
| chr12:48815429-48815620 | Common:1; Rare:44 | ||||
| chr12:48852127-48852344 | Common:2; Rare:63 | ||||
| chr12:48939726-48940028 | Common:2; Rare:70 | ||||
| chr12:49018736-49018947 | Common:1; Rare:88 | ||||
| chr12:49110663-49110787 | Rare:25 | ||||
| chr12:49131301-49131609 | Common:2; Rare:124 | ||||
| chr12:49188425-49188583 | Common:1; Rare:33 | ||||
| chr12:49188981-49189281 | Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264781-49265096 | Common:4; Rare:114 | ||||
| chr12:49322952-49323337 | Common:3; Rare:95 | ||||
| chr12:49366808-49367021 | Rare:51 | ||||
| chr12:49568104-49568192 | Common:2; Rare:29 | ||||
| chr12:49758245-49758460 | Common:4; Rare:67 |