| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6867361-6867680 | Common:2; Rare:149; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6869065-6869384 | Rare:98; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr12:6869464-6869773 | Common:1; Rare:85; Clinvar (pathogenic):1 | ||||
| chr12:6873274-6873705 | Common:4; Rare:122 | ||||
| chr12:6927613-6927834 | Rare:59 | ||||
| chr12:6928429-6928676 | Common:1; Rare:52 | ||||
| chr12:6937474-6937762 | Common:1; Rare:82 | ||||
| chr12:6943517-6943834 | Common:4; Rare:144 | ||||
| chr12:6943926-6944172 | Common:8; Rare:246; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6946335-6946635 | Common:1; Rare:77 | ||||
| chr12:6951268-6951407 | Rare:42 | ||||
| chr12:6967498-6967621 | Rare:49 | ||||
| chr12:6970195-6970372 | Rare:64 | ||||
| chr12:6970415-6970983 | Common:4; Rare:182; Clinvar (benign):1 | ||||
| chr12:6987543-6987799 | Rare:35 |