| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41446778-41446980 | Rare:85 | ||||
| chr22:41468939-41469175 | Rare:78 | ||||
| chr22:41621005-41621384 | Common:7; Rare:138 | ||||
| chr22:41753449-41753614 | Common:1; Rare:26 | ||||
| chr22:41800517-41800707 | Common:1; Rare:58 | ||||
| chr22:41832909-41833221 | Common:3; Rare:104 | ||||
| chr22:41898470-41898686 | Rare:60 | ||||
| chr22:41940206-41940417 | Common:1; Rare:42 | ||||
| chr22:42070646-42071047 | Common:4; Rare:94 | ||||
| chr22:42073927-42074301 | Common:5; Rare:85 | ||||
| chr22:42079629-42079832 | Common:1; Rare:70 | ||||
| chr22:42090668-42091001 | Common:2; Rare:148; Clinvar (pathogenic):1 | ||||
| chr22:42210684-42210925 | Rare:76 | ||||
| chr22:42432309-42432680 | Rare:84 | ||||
| chr22:42519778-42519874 | Common:1; Rare:40 |