| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49750380-49750782 | Rare:171 | ||||
| chr12:49827684-49828084 | Common:5; Rare:133 | ||||
| chr12:49828286-49829031 | Common:7; Rare:640 | ||||
| chr12:49842181-49843336 | Common:20; Rare:974; Clinvar (benign):5 | ||||
| chr12:49900271-49900375 | Rare:20 | ||||
| chr12:49966870-49967330 | Common:5; Rare:143 | ||||
| chr12:49967324-49967823 | Common:3; Rare:167 | ||||
| chr12:50024507-50024907 | Common:6; Rare:75 | ||||
| chr12:50024865-50025101 | Rare:67 | ||||
| chr12:50025362-50025835 | Common:11; Rare:560 | ||||
| chr12:50033420-50033710 | Common:3; Rare:65 | ||||
| chr12:50057410-50057830 | Common:1; Rare:127 | ||||
| chr12:50070479-50070950 | Common:6; Rare:151 | ||||
| chr12:50084770-50085430 | Common:6; Rare:529 | ||||
| chr12:50085420-50085790 | Common:3; Rare:243 |