| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:27973669-27973929 | Common:2; Rare:43 | ||||
| chr12:28130748-28131055 | Common:1; Rare:67 | ||||
| chr12:28899898-28899953 | Rare:13 | ||||
| chr12:45727520-45727608 | Rare:43 | ||||
| chr12:45727721-45727841 | Rare:46 | ||||
| chr12:46548915-46548974 | Rare:8 | ||||
| chr12:46549869-46550005 | Common:1; Rare:26 | ||||
| chr12:52147263-52147596 | Common:2; Rare:88 | ||||
| chr12:52148572-52148887 | Common:1; Rare:68 | ||||
| chr12:52280361-52280533 | Common:2; Rare:29 | ||||
| chr12:52280883-52281213 | Common:2; Rare:57 | ||||
| chr12:52488054-52488551 | Common:4; Rare:183; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:52496554-52496814 | Common:1; Rare:42 | ||||
| chr12:52496837-52497010 | Common:2; Rare:31 | ||||
| chr12:52514345-52514650 | Common:9; Rare:53; Clinvar:1; Clinvar (benign):1 |