| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:59597531-59597577 | Rare:7 | ||||
| chr12:62259389-62259431 | Rare:9 | ||||
| chr12:62259486-62259842 | Rare:74 | ||||
| chr12:62260047-62260471 | Common:1; Rare:156 | ||||
| chr12:62260767-62261092 | Rare:81 | ||||
| chr12:62466582-62466916 | Rare:94 | ||||
| chr12:62467231-62467372 | Common:1; Rare:42 | ||||
| chr12:63668438-63668789 | Common:5; Rare:100 | ||||
| chr12:63779780-63779963 | Common:2; Rare:66; Clinvar (benign):1 | ||||
| chr12:63780033-63780275 | Rare:108; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr12:63843994-63844123 | Common:3; Rare:24 | ||||
| chr12:64222191-64222413 | Common:1; Rare:79 | ||||
| chr12:64222495-64222614 | Rare:17 | ||||
| chr12:64404142-64404629 | Common:6; Rare:173 | ||||
| chr12:64404949-64405094 | Rare:33 |