| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42079497-42079771 | Common:2; Rare:74 | ||||
| chr22:42090686-42090972 | Common:2; Rare:125; Clinvar (pathogenic):1 | ||||
| chr22:42519764-42519913 | Common:1; Rare:62 | ||||
| chr22:42553717-42553923 | Common:1; Rare:62 | ||||
| chr22:42614853-42615244 | Common:3; Rare:159 | ||||
| chr22:42649324-42649482 | Common:1; Rare:63 | ||||
| chr22:42857178-42857471 | Common:3; Rare:124 | ||||
| chr22:43089297-43089531 | Common:4; Rare:78 | ||||
| chr22:43151447-43151590 | Common:2; Rare:33 | ||||
| chr22:43176134-43176350 | Common:3; Rare:88 | ||||
| chr22:43812202-43812441 | Common:3; Rare:82 | ||||
| chr22:43862389-43862642 | Common:8; Rare:105 | ||||
| chr22:43955303-43955566 | Common:3; Rare:80 | ||||
| chr22:44498080-44498449 | Common:3; Rare:132 | ||||
| chr22:45163694-45163991 | Common:4; Rare:106 |