| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38656340-38656744 | Common:1; Rare:109 | ||||
| chr22:38667820-38668126 | Common:1; Rare:53 | ||||
| chr22:38681778-38682438 | Common:3; Rare:226 | ||||
| chr22:38872191-38872438 | Rare:69 | ||||
| chr22:39014220-39014310 | Rare:26 | ||||
| chr22:39319566-39319707 | Common:2; Rare:78 | ||||
| chr22:39502158-39502374 | Rare:59 | ||||
| chr22:39532736-39533108 | Common:1; Rare:124 | ||||
| chr22:40044171-40044319 | Common:2; Rare:28 | ||||
| chr22:40044527-40044775 | Common:1; Rare:64 | ||||
| chr22:40346441-40346578 | Rare:61; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40856562-40857169 | Common:3; Rare:244; Clinvar:4 | ||||
| chr22:40951120-40951460 | Common:2; Rare:107 | ||||
| chr22:40951564-40951834 | Common:3; Rare:79 | ||||
| chr22:41286148-41286445 | Common:2; Rare:96 |