| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57772092-57772244 | Rare:53 | ||||
| chr12:57772539-57772636 | Common:2; Rare:13 | ||||
| chr12:57941360-57941704 | Common:3; Rare:102 | ||||
| chr12:58920139-58920362 | Common:2; Rare:69 | ||||
| chr12:58920496-58920704 | Common:2; Rare:70 | ||||
| chr12:59595934-59596206 | Common:5; Rare:63 | ||||
| chr12:62260032-62260441 | Common:1; Rare:154 | ||||
| chr12:63668828-63668927 | Common:2; Rare:16 | ||||
| chr12:63779729-63780169 | Common:3; Rare:178; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr12:64222242-64222384 | Rare:48 | ||||
| chr12:64404198-64404564 | Common:2; Rare:137 | ||||
| chr12:64452025-64452186 | Common:1; Rare:60 | ||||
| chr12:64610571-64610640 | Common:1; Rare:24 | ||||
| chr12:64759293-64759501 | Common:1; Rare:63; Clinvar:4 | ||||
| chr12:65169452-65169602 | Common:1; Rare:49; Clinvar:1 |