| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46286305-46286396 | Common:2; Rare:29 | ||||
| chr21:46323806-46324153 | Common:2; Rare:122; Clinvar (benign):1 | ||||
| chr21:46635480-46635689 | Common:4; Rare:67 | ||||
| chr22:17628698-17628866 | Common:1; Rare:55 | ||||
| chr22:17638696-17638817 | Rare:43 | ||||
| chr22:18077859-18078008 | Common:1; Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19178449-19178525 | Common:1; Rare:18 | ||||
| chr22:19432416-19432606 | Common:2; Rare:81 | ||||
| chr22:19854787-19854972 | Rare:63 | ||||
| chr22:19941657-19941877 | Rare:93; Clinvar:6; Clinvar (benign):7 | ||||
| chr22:20020899-20021134 | Common:1; Rare:77 | ||||
| chr22:20079964-20080292 | Common:1; Rare:110 | ||||
| chr22:20117259-20117577 | Common:2; Rare:98 | ||||
| chr22:20319998-20320125 | Common:1; Rare:49 | ||||
| chr22:20495781-20495966 | Common:2; Rare:71 |