| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56041563-56041968 | Common:4; Rare:88; Clinvar (benign):1 | ||||
| chr12:56116290-56116741 | Common:3; Rare:159 | ||||
| chr12:56117982-56118276 | Rare:97 | ||||
| chr12:56152460-56152630 | Rare:52 | ||||
| chr12:56189457-56189734 | Common:1; Rare:91 | ||||
| chr12:56221846-56222034 | Common:1; Rare:50 | ||||
| chr12:56300013-56300185 | Common:2; Rare:65 | ||||
| chr12:56300272-56300618 | Common:3; Rare:93 | ||||
| chr12:56315858-56316111 | Common:1; Rare:63 | ||||
| chr12:56333936-56334189 | Rare:78 | ||||
| chr12:56360088-56360405 | Common:3; Rare:74 | ||||
| chr12:56449376-56449478 | Rare:27 | ||||
| chr12:56468472-56468584 | Rare:52 | ||||
| chr12:56521849-56522021 | Common:2; Rare:34 | ||||
| chr12:56636334-56636447 | Rare:19 |