| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40044528-40044865 | Common:4; Rare:142 | ||||
| chr22:40177551-40178022 | Rare:180 | ||||
| chr22:40346434-40346582 | Rare:120; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr22:40636638-40637035 | Common:4; Rare:218 | ||||
| chr22:40856436-40856724 | Rare:202 | ||||
| chr22:40856831-40857203 | Common:5; Rare:254; Clinvar:8 | ||||
| chr22:40951056-40951423 | Common:4; Rare:240 | ||||
| chr22:40951440-40951840 | Common:6; Rare:187 | ||||
| chr22:41091430-41091849 | Common:12; Rare:295 | ||||
| chr22:41286105-41286560 | Common:4; Rare:274 | ||||
| chr22:41301473-41301636 | Rare:95 | ||||
| chr22:41367090-41367380 | Rare:75 | ||||
| chr22:41381210-41381600 | Common:11; Rare:241 | ||||
| chr22:41381695-41382017 | Common:7; Rare:221 | ||||
| chr22:41446780-41447003 | Rare:185 |