| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38656374-38656716 | Common:1; Rare:85 | ||||
| chr22:38681836-38682221 | Common:1; Rare:148 | ||||
| chr22:38794082-38794309 | Common:1; Rare:61 | ||||
| chr22:38872178-38872471 | Rare:78 | ||||
| chr22:38982097-38982444 | Common:3; Rare:78 | ||||
| chr22:39319526-39319856 | Common:3; Rare:146 | ||||
| chr22:39320305-39320392 | Common:1; Rare:23 | ||||
| chr22:39399646-39399808 | Common:3; Rare:66 | ||||
| chr22:39502158-39502412 | Rare:75 | ||||
| chr22:39532667-39533055 | Common:2; Rare:148 | ||||
| chr22:39533071-39533107 | Rare:7 | ||||
| chr22:40044121-40044350 | Common:2; Rare:52 | ||||
| chr22:40044527-40044871 | Common:2; Rare:81 | ||||
| chr22:40177788-40177977 | Rare:62 | ||||
| chr22:40346427-40346603 | Rare:88; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):1 |