| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17628699-17628997 | Common:1; Rare:99 | ||||
| chr22:17638668-17638819 | Rare:52 | ||||
| chr22:18077780-18078014 | Common:4; Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19291707-19291938 | Common:9; Rare:68 | ||||
| chr22:19432303-19432606 | Common:4; Rare:129 | ||||
| chr22:19447671-19447853 | Common:2; Rare:78 | ||||
| chr22:19854796-19855013 | Rare:81 | ||||
| chr22:20020897-20021145 | Common:1; Rare:82 | ||||
| chr22:20116959-20117013 | Common:1; Rare:9 | ||||
| chr22:20117167-20117571 | Common:3; Rare:129 | ||||
| chr22:20319998-20320107 | Common:1; Rare:43 | ||||
| chr22:20495781-20495917 | Common:1; Rare:53 | ||||
| chr22:20583210-20583462 | Common:1; Rare:71 | ||||
| chr22:20982216-20982358 | Common:1; Rare:30; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:21002098-21002201 | Common:3; Rare:34 |