| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39893716-39893827 | Rare:23 | ||||
| chr22:40044121-40044386 | Common:2; Rare:66 | ||||
| chr22:40044517-40044979 | Common:3; Rare:116 | ||||
| chr22:40177872-40178046 | Rare:42 | ||||
| chr22:40346433-40346649 | Rare:101; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:40370530-40370682 | Rare:62 | ||||
| chr22:40636621-40637020 | Common:2; Rare:115 | ||||
| chr22:40819232-40819499 | Common:11; Rare:128 | ||||
| chr22:40856316-40857169 | Common:4; Rare:345; Clinvar:4 | ||||
| chr22:40951056-40951475 | Common:2; Rare:136 | ||||
| chr22:40951598-40951858 | Common:2; Rare:75 | ||||
| chr22:41091394-41091862 | Common:6; Rare:175 | ||||
| chr22:41148837-41149142 | Common:3; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:41158300-41158494 | Rare:40; Clinvar (pathogenic):1 | ||||
| chr22:41205079-41205384 | Common:2; Rare:92 |