| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57752235-57752720 | Common:1; Rare:128; Clinvar:1 | ||||
| chr12:57754837-57755141 | Common:2; Rare:74 | ||||
| chr12:57755277-57755536 | Rare:63 | ||||
| chr12:57755993-57756078 | Rare:22 | ||||
| chr12:57765135-57765409 | Common:1; Rare:105; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr12:57765490-57765530 | Rare:15 | ||||
| chr12:57765544-57765606 | Rare:29 | ||||
| chr12:57771725-57771941 | Rare:44 | ||||
| chr12:57772032-57772439 | Common:2; Rare:118 | ||||
| chr12:57772447-57772736 | Common:4; Rare:67 | ||||
| chr12:57772739-57772912 | Common:1; Rare:43 | ||||
| chr12:57772942-57773000 | Rare:16 | ||||
| chr12:57782644-57782862 | Common:2; Rare:82; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:57845101-57845141 | Rare:6 | ||||
| chr12:57845451-57845916 | Common:4; Rare:114 |