| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54259503-54259638 | Rare:27 | ||||
| chr12:54279665-54279958 | Common:2; Rare:95 | ||||
| chr12:54280027-54280320 | Rare:94 | ||||
| chr12:54281140-54281516 | Common:4; Rare:122 | ||||
| chr12:54282092-54282486 | Rare:90 | ||||
| chr12:54283799-54284338 | Common:2; Rare:150; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
| chr12:55715942-55715973 | Rare:12 | ||||
| chr12:55715997-55716195 | Common:2; Rare:93 | ||||
| chr12:55716225-55716588 | Common:3; Rare:92 | ||||
| chr12:55728283-55728514 | Rare:73 | ||||
| chr12:55728939-55729226 | Rare:62 | ||||
| chr12:55729650-55729813 | Rare:35 | ||||
| chr12:55829491-55829793 | Rare:94 | ||||
| chr12:55931944-55932101 | Rare:41 | ||||
| chr12:55966698-55966885 | Rare:48 |