| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43891999-43892328 | Common:1; Rare:59 | ||||
| chr22:43923496-43923835 | Common:5; Rare:89; Clinvar (benign):3 | ||||
| chr22:43955311-43955583 | Common:3; Rare:82 | ||||
| chr22:44024214-44024323 | Rare:42 | ||||
| chr22:44498149-44498479 | Common:2; Rare:121 | ||||
| chr22:44752437-44752620 | Common:4; Rare:64 | ||||
| chr22:44968672-44968928 | Rare:41 | ||||
| chr22:45008913-45008981 | Rare:20 | ||||
| chr22:45009919-45010127 | Common:1; Rare:84 | ||||
| chr22:45163654-45163952 | Common:4; Rare:100 | ||||
| chr22:45164064-45164246 | Common:2; Rare:64 | ||||
| chr22:45413624-45413766 | Common:1; Rare:47 | ||||
| chr22:45502544-45502943 | Common:2; Rare:115 | ||||
| chr22:46250235-46250413 | Common:3; Rare:51 | ||||
| chr22:46267870-46268037 | Common:1; Rare:52 |