| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41286175-41286424 | Common:2; Rare:74 | ||||
| chr22:41469055-41469317 | Rare:118 | ||||
| chr22:41621051-41621370 | Common:7; Rare:115 | ||||
| chr22:41800506-41800631 | Rare:40 | ||||
| chr22:41832909-41833291 | Common:3; Rare:137 | ||||
| chr22:42070779-42070948 | Common:2; Rare:35 | ||||
| chr22:42079634-42079774 | Common:1; Rare:42 | ||||
| chr22:42090664-42090953 | Common:2; Rare:128; Clinvar (pathogenic):1 | ||||
| chr22:42210684-42210924 | Rare:76 | ||||
| chr22:42614857-42615246 | Common:3; Rare:161 | ||||
| chr22:42649322-42649479 | Common:1; Rare:62 | ||||
| chr22:42857178-42857430 | Common:3; Rare:105 | ||||
| chr22:43015087-43015384 | Common:2; Rare:121 | ||||
| chr22:43812223-43812441 | Common:3; Rare:73 | ||||
| chr22:43955338-43955562 | Common:2; Rare:69 |