| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17638696-17638830 | Rare:49 | ||||
| chr22:17774404-17774569 | Rare:58 | ||||
| chr22:18077859-18078032 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19291714-19291940 | Common:9; Rare:67 | ||||
| chr22:19432322-19432569 | Common:3; Rare:99 | ||||
| chr22:19447667-19447775 | Common:1; Rare:55 | ||||
| chr22:19479142-19479448 | Common:4; Rare:108 | ||||
| chr22:19854787-19855013 | Rare:83 | ||||
| chr22:19941764-19941877 | Rare:46; Clinvar:2 | ||||
| chr22:19963102-19963292 | Common:1; Rare:47 | ||||
| chr22:20020883-20021151 | Common:1; Rare:89 | ||||
| chr22:20079914-20080253 | Common:1; Rare:108 | ||||
| chr22:20117179-20117571 | Common:3; Rare:124 | ||||
| chr22:20319989-20320174 | Common:2; Rare:64 | ||||
| chr22:20495771-20495904 | Common:1; Rare:48 |