| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:18149722-18150008 | Common:1; Rare:51 | ||||
| chr22:19122360-19122650 | Common:4; Rare:75 | ||||
| chr22:19178456-19178521 | Common:1; Rare:16 | ||||
| chr22:19178717-19179028 | Common:4; Rare:108 | ||||
| chr22:19187699-19188010 | Rare:81 | ||||
| chr22:19291657-19291940 | Common:11; Rare:98 | ||||
| chr22:19431711-19431828 | Rare:28 | ||||
| chr22:19432314-19432610 | Common:4; Rare:127 | ||||
| chr22:19447685-19447931 | Common:2; Rare:98 | ||||
| chr22:19479096-19479471 | Common:4; Rare:139 | ||||
| chr22:19479693-19479959 | Common:4; Rare:73 | ||||
| chr22:19854788-19855041 | Common:1; Rare:93 | ||||
| chr22:19941708-19941893 | Rare:80; Clinvar:6; Clinvar (benign):4 | ||||
| chr22:20080050-20080301 | Rare:91 | ||||
| chr22:20116925-20117612 | Common:4; Rare:207 |