| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:18150068-18150188 | Common:1; Rare:35 | ||||
| chr22:18906162-18906352 | Common:1; Rare:27 | ||||
| chr22:19178419-19178536 | Common:1; Rare:36 | ||||
| chr22:19291696-19291942 | Common:10; Rare:74 | ||||
| chr22:19432399-19432614 | Common:2; Rare:89 | ||||
| chr22:19447667-19447876 | Common:2; Rare:90 | ||||
| chr22:19479107-19479466 | Common:4; Rare:132 | ||||
| chr22:19524398-19524653 | Common:1; Rare:79 | ||||
| chr22:19854782-19854979 | Common:1; Rare:67 | ||||
| chr22:19941715-19941892 | Rare:76; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20020884-20021176 | Common:1; Rare:94 | ||||
| chr22:20079930-20080288 | Common:1; Rare:117 | ||||
| chr22:20116941-20117571 | Common:4; Rare:184 | ||||
| chr22:20319994-20320158 | Common:2; Rare:53 | ||||
| chr22:20393950-20394194 | Common:1; Rare:75 |