| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:18150040-18150176 | Common:1; Rare:37 | ||||
| chr22:19122389-19122699 | Common:3; Rare:77 | ||||
| chr22:19432327-19432626 | Common:2; Rare:125 | ||||
| chr22:19447684-19447931 | Common:2; Rare:98 | ||||
| chr22:19479112-19479471 | Common:4; Rare:130 | ||||
| chr22:19854791-19855023 | Rare:87 | ||||
| chr22:19941722-19941886 | Rare:69; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20020899-20021134 | Common:1; Rare:77 | ||||
| chr22:20079930-20080279 | Common:1; Rare:113 | ||||
| chr22:20117135-20117652 | Common:4; Rare:167 | ||||
| chr22:20319989-20320158 | Common:2; Rare:57 | ||||
| chr22:20495781-20495904 | Common:1; Rare:47 | ||||
| chr22:20507496-20507622 | Rare:28 | ||||
| chr22:20858699-20859102 | Common:6; Rare:204; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:20982190-20982358 | Common:2; Rare:41; Clinvar (benign):2; Clinvar (pathogenic):1 |