| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64451951-64452372 | Common:1; Rare:146 | ||||
| chr12:64759364-64759496 | Common:1; Rare:43; Clinvar:3 | ||||
| chr12:65169476-65169605 | Common:1; Rare:44; Clinvar:1 | ||||
| chr12:65278455-65278779 | Common:3; Rare:101; Clinvar (benign):1 | ||||
| chr12:65278815-65278833 | Rare:7; Clinvar (benign):1 | ||||
| chr12:65823938-65823974 | Rare:9 | ||||
| chr12:65824275-65824536 | Common:1; Rare:63 | ||||
| chr12:65824596-65824910 | Common:7; Rare:105 | ||||
| chr12:65824944-65825265 | Rare:80 | ||||
| chr12:66130703-66130861 | Rare:57 | ||||
| chr12:67269325-67269671 | Common:1; Rare:105 | ||||
| chr12:67648539-67648802 | Common:3; Rare:69 | ||||
| chr12:68332265-68332533 | Common:1; Rare:88 | ||||
| chr12:68610704-68611028 | Common:1; Rare:141 | ||||
| chr12:68686814-68687048 | Common:4; Rare:71 |