| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38570147-38570438 | Common:4; Rare:52 | ||||
| chr22:38656288-38656683 | Common:1; Rare:111 | ||||
| chr22:38681847-38682045 | Common:1; Rare:87 | ||||
| chr22:38705864-38706015 | Rare:50 | ||||
| chr22:38794088-38794363 | Common:1; Rare:73 | ||||
| chr22:38872191-38872394 | Rare:59 | ||||
| chr22:39319486-39319779 | Common:5; Rare:133 | ||||
| chr22:39399727-39399796 | Common:1; Rare:31 | ||||
| chr22:39502162-39502412 | Rare:74 | ||||
| chr22:40044552-40044883 | Common:2; Rare:74 | ||||
| chr22:40177731-40177992 | Rare:79 | ||||
| chr22:40346441-40346702 | Common:1; Rare:113; Clinvar:12; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:40636659-40637012 | Common:2; Rare:96 | ||||
| chr22:40819268-40819553 | Common:11; Rare:126 | ||||
| chr22:40856434-40856477 | Rare:15 |