| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6851239-6851504 | Rare:63 | ||||
| chr12:6851913-6852185 | Rare:69 | ||||
| chr12:6867334-6867358 | Rare:4 | ||||
| chr12:6867381-6867678 | Common:2; Rare:141; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6867994-6868165 | Common:5; Rare:71 | ||||
| chr12:6873230-6873739 | Common:5; Rare:140 | ||||
| chr12:6904703-6905047 | Common:2; Rare:80 | ||||
| chr12:6924887-6925156 | Common:11; Rare:67 | ||||
| chr12:6927248-6927813 | Rare:125 | ||||
| chr12:6942278-6942594 | Common:3; Rare:75 | ||||
| chr12:6943517-6943964 | Common:15; Rare:298 | ||||
| chr12:6943978-6944173 | Common:3; Rare:191; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6946342-6946670 | Common:1; Rare:89 | ||||
| chr12:6970393-6970993 | Common:5; Rare:191; Clinvar (benign):1 | ||||
| chr12:7018408-7018714 | Common:1; Rare:89 |