| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20917181-20917484 | Rare:115 | ||||
| chr22:20917638-20917901 | Common:1; Rare:64 | ||||
| chr22:20982196-20982347 | Common:2; Rare:34; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002088-21002215 | Common:3; Rare:49 | ||||
| chr22:21629982-21630262 | Common:2; Rare:94 | ||||
| chr22:21938159-21938300 | Rare:49 | ||||
| chr22:23690343-23690456 | Rare:23 | ||||
| chr22:23750941-23751206 | Common:3; Rare:88 | ||||
| chr22:23767892-23768046 | Rare:44 | ||||
| chr22:23838983-23839207 | Rare:74 | ||||
| chr22:23857651-23857914 | Common:2; Rare:90 | ||||
| chr22:23894198-23894517 | Common:4; Rare:115 | ||||
| chr22:24270697-24271166 | Common:5; Rare:173 | ||||
| chr22:24543965-24544265 | Common:2; Rare:83 | ||||
| chr22:24555614-24556045 | Rare:136 |