| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57693877-57694191 | Common:1; Rare:87 | ||||
| chr12:57694573-57694838 | Rare:62 | ||||
| chr12:57744851-57745093 | Common:1; Rare:51 | ||||
| chr12:57745341-57745376 | Rare:6 | ||||
| chr12:57752249-57752627 | Rare:107; Clinvar:1 | ||||
| chr12:57771592-57771911 | Common:1; Rare:76 | ||||
| chr12:57772072-57772262 | Rare:69 | ||||
| chr12:57772528-57772670 | Common:3; Rare:21 | ||||
| chr12:57782422-57782838 | Common:3; Rare:109; Clinvar (benign):3 | ||||
| chr12:57783005-57783156 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr12:57845504-57845557 | Rare:15 | ||||
| chr12:57846376-57846476 | Rare:32 | ||||
| chr12:57846906-57847221 | Common:2; Rare:113 | ||||
| chr12:57941405-57941738 | Common:3; Rare:102 | ||||
| chr12:58920153-58920366 | Common:2; Rare:65 |