| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17628623-17628852 | Common:2; Rare:77 | ||||
| chr22:17774384-17774569 | Rare:63 | ||||
| chr22:18077814-18078065 | Common:5; Rare:78; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:18150054-18150188 | Common:1; Rare:36 | ||||
| chr22:19447686-19447977 | Common:2; Rare:112 | ||||
| chr22:19479611-19479952 | Common:5; Rare:82 | ||||
| chr22:19854813-19855064 | Common:1; Rare:95 | ||||
| chr22:19941709-19941881 | Rare:74; Clinvar:6; Clinvar (benign):4 | ||||
| chr22:20117116-20117587 | Common:3; Rare:149 | ||||
| chr22:20319979-20320146 | Common:2; Rare:60 | ||||
| chr22:20495781-20495999 | Common:2; Rare:82 | ||||
| chr22:20507488-20507630 | Rare:34 | ||||
| chr22:20858744-20859093 | Common:5; Rare:175; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:20917170-20917469 | Rare:112 | ||||
| chr22:20982201-20982352 | Common:2; Rare:33; Clinvar (benign):2; Clinvar (pathogenic):1 |