| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19479687-19479928 | Common:3; Rare:53 | ||||
| chr22:19720203-19720408 | Rare:61 | ||||
| chr22:19854811-19855023 | Rare:83 | ||||
| chr22:20020873-20021145 | Common:1; Rare:90 | ||||
| chr22:20079921-20080299 | Common:1; Rare:125 | ||||
| chr22:20117175-20117594 | Common:3; Rare:135 | ||||
| chr22:20319972-20320202 | Common:2; Rare:85 | ||||
| chr22:20393948-20394204 | Common:1; Rare:81 | ||||
| chr22:20495771-20496019 | Common:2; Rare:88 | ||||
| chr22:20496203-20496230 | Rare:4 | ||||
| chr22:20507490-20507668 | Rare:65 | ||||
| chr22:20858259-20858437 | Common:2; Rare:40 | ||||
| chr22:20858704-20859093 | Common:6; Rare:196; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:20917112-20917529 | Rare:145 | ||||
| chr22:20981867-20981989 | Common:1; Rare:30 |