| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6451795-6452150 | Common:4; Rare:67 | ||||
| chr12:6470672-6470922 | Common:1; Rare:61 | ||||
| chr12:6493132-6493502 | Common:8; Rare:116 | ||||
| chr12:6493770-6494149 | Common:2; Rare:111 | ||||
| chr12:6534219-6534578 | Common:6; Rare:137 | ||||
| chr12:6568224-6568388 | Rare:61 | ||||
| chr12:6688897-6688973 | Rare:17 | ||||
| chr12:6689242-6689755 | Common:3; Rare:142 | ||||
| chr12:6723968-6724291 | Rare:80 | ||||
| chr12:6752937-6753189 | Common:6; Rare:77 | ||||
| chr12:6851236-6851452 | Rare:52 | ||||
| chr12:6851913-6852174 | Rare:66 | ||||
| chr12:6869483-6869773 | Common:1; Rare:83; Clinvar (pathogenic):1 | ||||
| chr12:6873282-6873617 | Common:3; Rare:95 | ||||
| chr12:6943676-6944172 | Common:17; Rare:445; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 |