| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38656236-38656721 | Common:1; Rare:131 | ||||
| chr22:38681789-38682246 | Common:3; Rare:172 | ||||
| chr22:38794069-38794282 | Common:1; Rare:59 | ||||
| chr22:38872180-38872561 | Rare:110 | ||||
| chr22:39244958-39245334 | Common:1; Rare:79 | ||||
| chr22:39319578-39319896 | Common:4; Rare:122 | ||||
| chr22:39349769-39350025 | Common:1; Rare:77 | ||||
| chr22:39399503-39399805 | Common:4; Rare:105 | ||||
| chr22:39502041-39502412 | Rare:103 | ||||
| chr22:39532672-39533009 | Common:2; Rare:135 | ||||
| chr22:40044160-40044346 | Common:2; Rare:37 | ||||
| chr22:40044528-40044866 | Common:2; Rare:79 | ||||
| chr22:40177752-40178011 | Rare:77 | ||||
| chr22:40346433-40346556 | Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40370506-40370682 | Rare:71 |