| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20917170-20917516 | Rare:125 | ||||
| chr22:20982204-20982433 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr22:21002049-21002232 | Common:3; Rare:71 | ||||
| chr22:21694410-21694635 | Common:3; Rare:72 | ||||
| chr22:21867643-21867794 | Common:1; Rare:37 | ||||
| chr22:23690383-23690595 | Common:1; Rare:48 | ||||
| chr22:23751095-23751209 | Common:1; Rare:39 | ||||
| chr22:23894238-23894817 | Common:6; Rare:217 | ||||
| chr22:24244245-24244593 | Common:9; Rare:118 | ||||
| chr22:24270800-24271174 | Common:5; Rare:144 | ||||
| chr22:24554951-24555484 | Common:4; Rare:199 | ||||
| chr22:24555617-24556068 | Rare:138 | ||||
| chr22:26483779-26483923 | Common:4; Rare:56; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:26512364-26512588 | Common:2; Rare:86 | ||||
| chr22:26590061-26590220 | Common:3; Rare:70 |