| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41947083-41947204 | Common:1; Rare:43 | ||||
| chr22:41998602-41998811 | Common:2; Rare:76 | ||||
| chr22:42070523-42070980 | Common:4; Rare:105; Clinvar:1 | ||||
| chr22:42079616-42079843 | Common:1; Rare:82 | ||||
| chr22:42090675-42091073 | Common:2; Rare:158; Clinvar (pathogenic):1 | ||||
| chr22:42519610-42519899 | Common:2; Rare:117 | ||||
| chr22:42614824-42615246 | Common:3; Rare:182 | ||||
| chr22:42649313-42649488 | Common:1; Rare:71 | ||||
| chr22:42720813-42720946 | Rare:42 | ||||
| chr22:42857178-42857422 | Common:3; Rare:102 | ||||
| chr22:42959815-42959985 | Common:1; Rare:32 | ||||
| chr22:43015087-43015384 | Common:2; Rare:121 | ||||
| chr22:43089338-43089496 | Common:3; Rare:50 | ||||
| chr22:43151357-43151607 | Common:3; Rare:61 | ||||
| chr22:43812242-43812478 | Common:4; Rare:84 |