| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41620970-41621375 | Common:7; Rare:142 | ||||
| chr22:41621721-41622086 | Common:1; Rare:92 | ||||
| chr22:41800506-41800699 | Common:1; Rare:61 | ||||
| chr22:41832557-41832626 | Rare:7 | ||||
| chr22:41832909-41833355 | Common:3; Rare:149 | ||||
| chr22:41946683-41946977 | Common:3; Rare:76 | ||||
| chr22:41947089-41947255 | Rare:57 | ||||
| chr22:42070768-42071049 | Common:3; Rare:64 | ||||
| chr22:42079616-42079839 | Common:1; Rare:81 | ||||
| chr22:42090607-42090949 | Common:2; Rare:146; Clinvar (pathogenic):1 | ||||
| chr22:42519610-42519913 | Common:2; Rare:122 | ||||
| chr22:42614840-42615265 | Common:3; Rare:186 | ||||
| chr22:42649322-42649593 | Common:6; Rare:96 | ||||
| chr22:42857151-42857452 | Common:3; Rare:121 | ||||
| chr22:43015087-43015384 | Common:2; Rare:121 |