| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:28741791-28742078 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):3 | ||||
| chr22:28742402-28742701 | Common:1; Rare:73 | ||||
| chr22:28800019-28800744 | Common:7; Rare:245 | ||||
| chr22:29267931-29268339 | Common:2; Rare:119 | ||||
| chr22:29767060-29767399 | Common:4; Rare:107 | ||||
| chr22:30289498-30289861 | Common:3; Rare:89 | ||||
| chr22:30326877-30327174 | Common:2; Rare:104 | ||||
| chr22:30356860-30357026 | Common:1; Rare:53 | ||||
| chr22:30591856-30592197 | Common:5; Rare:101 | ||||
| chr22:30606982-30607319 | Common:3; Rare:111; Clinvar:4; Clinvar (benign):3 | ||||
| chr22:31081130-31081351 | Common:1; Rare:59 | ||||
| chr22:31082957-31083207 | Common:1; Rare:54 | ||||
| chr22:31107480-31107821 | Common:2; Rare:110 | ||||
| chr22:31248186-31248434 | Common:1; Rare:52 | ||||
| chr22:31290718-31290922 | Rare:85 |