| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:45163632-45164147 | Common:7; Rare:189 | ||||
| chr22:45235203-45235279 | Common:3; Rare:16 | ||||
| chr22:45235324-45235649 | Common:5; Rare:98 | ||||
| chr22:45240824-45241093 | Common:2; Rare:52 | ||||
| chr22:45309467-45310164 | Common:3; Rare:243 | ||||
| chr22:45671736-45672103 | Common:3; Rare:138 | ||||
| chr22:46250115-46250595 | Common:6; Rare:136 | ||||
| chr22:46267745-46268109 | Common:2; Rare:107 | ||||
| chr22:46288361-46288581 | Rare:72 | ||||
| chr22:46296402-46296476 | Rare:20 | ||||
| chr22:46296481-46296925 | Common:4; Rare:125 | ||||
| chr22:46335550-46335836 | Common:6; Rare:125; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr22:46336535-46336559 | Common:1; Rare:4 | ||||
| chr22:46576965-46577155 | Common:1; Rare:75 | ||||
| chr22:46737433-46737649 | Rare:48 |