| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39532668-39533053 | Common:2; Rare:148 | ||||
| chr22:40044552-40044871 | Common:2; Rare:72 | ||||
| chr22:40177686-40177946 | Rare:71 | ||||
| chr22:40346427-40346580 | Rare:70; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40636668-40637031 | Common:2; Rare:102 | ||||
| chr22:40819301-40819498 | Common:11; Rare:103 | ||||
| chr22:40856567-40857169 | Common:3; Rare:238; Clinvar:4 | ||||
| chr22:41286142-41286486 | Common:2; Rare:110 | ||||
| chr22:41468719-41469149 | Rare:101 | ||||
| chr22:41544440-41544718 | Common:3; Rare:81 | ||||
| chr22:41621006-41621373 | Common:7; Rare:135 | ||||
| chr22:41621582-41621810 | Common:2; Rare:68 | ||||
| chr22:41800506-41800638 | Rare:43 | ||||
| chr22:41832828-41833203 | Common:3; Rare:119 | ||||
| chr22:41947093-41947243 | Rare:55 |