| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56221822-56222026 | Common:2; Rare:52 | ||||
| chr12:56224112-56224512 | Common:3; Rare:110 | ||||
| chr12:56224517-56224800 | Common:1; Rare:71 | ||||
| chr12:56258331-56258477 | Rare:47 | ||||
| chr12:56285987-56286201 | Common:1; Rare:41 | ||||
| chr12:56299997-56300154 | Common:2; Rare:58 | ||||
| chr12:56300244-56300573 | Common:1; Rare:98 | ||||
| chr12:56315865-56316115 | Common:1; Rare:64 | ||||
| chr12:56333928-56334161 | Rare:65 | ||||
| chr12:56349340-56349628 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:56350840-56351118 | Common:1; Rare:67 | ||||
| chr12:56360062-56360445 | Common:4; Rare:87 | ||||
| chr12:56468418-56468676 | Common:1; Rare:105 | ||||
| chr12:56521944-56522052 | Common:1; Rare:29 | ||||
| chr12:56645901-56646283 | Common:1; Rare:99 |