| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:54358881-54359529 | Common:3; Rare:145 | ||||
| chr12:56169589-56169801 | Rare:60 | ||||
| chr12:56247493-56247751 | Rare:70 | ||||
| chr12:56634970-56635091 | Common:1; Rare:21 | ||||
| chr12:57239142-57239416 | Common:1; Rare:62 | ||||
| chr12:57569047-57569332 | Common:3; Rare:72; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr12:57935906-57936256 | Common:4; Rare:88 | ||||
| chr12:62603435-62603794 | Common:1; Rare:117 | ||||
| chr12:64825269-64825461 | Common:1; Rare:52 | ||||
| chr12:64825953-64826005 | Rare:12 | ||||
| chr12:64826408-64826542 | Common:1; Rare:28 | ||||
| chr12:65170288-65170550 | Common:1; Rare:111; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:67069628-67069703 | Rare:23 | ||||
| chr12:67519890-67520057 | Rare:30 | ||||
| chr12:67520062-67520137 | Rare:19 |