| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41281557-41281764 | Rare:46 | ||||
| chr22:41285869-41286058 | Common:1; Rare:47 | ||||
| chr22:41286109-41286444 | Common:2; Rare:108 | ||||
| chr22:41301143-41301472 | Common:2; Rare:83 | ||||
| chr22:41367133-41367493 | Rare:98 | ||||
| chr22:41381247-41381438 | Common:4; Rare:67 | ||||
| chr22:41381714-41382054 | Common:3; Rare:133 | ||||
| chr22:41446790-41446963 | Rare:70 | ||||
| chr22:41468589-41469045 | Common:2; Rare:99 | ||||
| chr22:41469056-41469167 | Rare:53 | ||||
| chr22:41515106-41515496 | Rare:70; Clinvar:1; Clinvar (benign):3 | ||||
| chr22:41544314-41544871 | Common:12; Rare:175 | ||||
| chr22:41560908-41561133 | Common:9; Rare:64 | ||||
| chr22:41604091-41604393 | Common:1; Rare:62 | ||||
| chr22:41690459-41690587 | Rare:25 |