| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17628703-17628833 | Common:1; Rare:44 | ||||
| chr22:17638674-17638817 | Rare:50 | ||||
| chr22:18077820-18078022 | Common:4; Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19144639-19144928 | Common:5; Rare:97 | ||||
| chr22:19432303-19432606 | Common:4; Rare:129 | ||||
| chr22:19447677-19447860 | Common:2; Rare:76 | ||||
| chr22:19479116-19479471 | Common:4; Rare:128 | ||||
| chr22:19479665-19479975 | Common:5; Rare:85 | ||||
| chr22:19854811-19855024 | Rare:84 | ||||
| chr22:19941722-19941877 | Rare:66; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20020873-20021131 | Common:1; Rare:84 | ||||
| chr22:20079916-20080292 | Common:1; Rare:120 | ||||
| chr22:20117159-20117655 | Common:4; Rare:163 | ||||
| chr22:20319989-20320104 | Common:2; Rare:46 | ||||
| chr22:20393952-20394197 | Common:1; Rare:76 |