| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39319586-39319768 | Common:3; Rare:83 | ||||
| chr22:39502158-39502412 | Rare:75 | ||||
| chr22:39532672-39533055 | Common:2; Rare:148 | ||||
| chr22:40044174-40044334 | Common:2; Rare:30 | ||||
| chr22:40044555-40044874 | Common:2; Rare:72 | ||||
| chr22:40346445-40346578 | Rare:60; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40636629-40637014 | Common:2; Rare:110 | ||||
| chr22:40856369-40856700 | Common:1; Rare:157 | ||||
| chr22:40856957-40857158 | Rare:90; Clinvar:3 | ||||
| chr22:40951031-40951441 | Common:2; Rare:140 | ||||
| chr22:40951595-40951716 | Common:1; Rare:35 | ||||
| chr22:41091413-41091862 | Common:6; Rare:166 | ||||
| chr22:41286158-41286547 | Common:2; Rare:120 | ||||
| chr22:41367224-41367465 | Rare:75 | ||||
| chr22:41446486-41446571 | Rare:17 |