| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20319994-20320160 | Common:2; Rare:54 | ||||
| chr22:20393950-20394239 | Common:1; Rare:84 | ||||
| chr22:20429325-20429495 | Common:1; Rare:64 | ||||
| chr22:20495775-20495925 | Common:2; Rare:56 | ||||
| chr22:20507490-20507643 | Rare:45 | ||||
| chr22:20858937-20859093 | Common:3; Rare:86; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:20917278-20917413 | Rare:47 | ||||
| chr22:20982209-20982535 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr22:21002061-21002215 | Common:3; Rare:62 | ||||
| chr22:21032554-21032632 | Rare:32 | ||||
| chr22:21651914-21652192 | Common:2; Rare:58 | ||||
| chr22:21665948-21666070 | Rare:36 | ||||
| chr22:21952792-21952982 | Common:1; Rare:70 | ||||
| chr22:21982740-21982865 | Rare:33 | ||||
| chr22:22508703-22508908 | Rare:67 |