| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54364463-54364634 | Common:3; Rare:29 | ||||
| chr12:54384571-54384859 | Common:2; Rare:52 | ||||
| chr12:54419005-54419312 | Rare:96 | ||||
| chr12:54419449-54419662 | Rare:36 | ||||
| chr12:54497505-54497870 | Rare:72 | ||||
| chr12:54561205-54561569 | Common:2; Rare:61 | ||||
| chr12:55681314-55681584 | Common:2; Rare:45 | ||||
| chr12:55707480-55707633 | Rare:58; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:55712086-55712425 | Common:7; Rare:80; Clinvar (benign):1 | ||||
| chr12:55716000-55716227 | Common:2; Rare:97 | ||||
| chr12:55716319-55716588 | Common:3; Rare:67 | ||||
| chr12:55720184-55720443 | Common:4; Rare:35; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:55720953-55721159 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chr12:55727124-55727465 | Rare:101 | ||||
| chr12:55728275-55728553 | Rare:82 |