| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53467714-53468143 | Common:1; Rare:100 | ||||
| chr12:53468705-53468833 | Rare:37 | ||||
| chr12:53500695-53500959 | Common:2; Rare:52 | ||||
| chr12:53501128-53501195 | Rare:20 | ||||
| chr12:53501197-53501459 | Rare:66 | ||||
| chr12:53501543-53501661 | Rare:30 | ||||
| chr12:53676033-53676151 | Common:1; Rare:67 | ||||
| chr12:53676155-53676181 | Rare:10 | ||||
| chr12:53938456-53938921 | Common:6; Rare:122 | ||||
| chr12:53984986-53985227 | Common:2; Rare:57 | ||||
| chr12:54008949-54009013 | Rare:13 | ||||
| chr12:54016932-54017200 | Common:1; Rare:60 | ||||
| chr12:54053777-54053863 | Rare:9 | ||||
| chr12:54259500-54259652 | Rare:32 | ||||
| chr12:54283750-54284138 | Common:1; Rare:104; Clinvar:2; Clinvar (pathogenic):6 |