| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:21867564-21867823 | Common:4; Rare:84 | ||||
| chr22:21868000-21868215 | Common:2; Rare:45 | ||||
| chr22:21938103-21938359 | Rare:81 | ||||
| chr22:21982702-21982924 | Rare:61 | ||||
| chr22:22508705-22508928 | Common:1; Rare:73 | ||||
| chr22:23138357-23138533 | Common:2; Rare:34 | ||||
| chr22:23180724-23180828 | Common:2; Rare:48 | ||||
| chr22:23751071-23751299 | Common:3; Rare:71 | ||||
| chr22:23751409-23751620 | Common:1; Rare:40 | ||||
| chr22:23754379-23754564 | Common:3; Rare:45 | ||||
| chr22:23763649-23763778 | Rare:31 | ||||
| chr22:23767875-23768082 | Rare:59 | ||||
| chr22:23772723-23772921 | Common:1; Rare:72 | ||||
| chr22:23786857-23787088 | Common:2; Rare:87; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:23787206-23787524 | Common:7; Rare:126; Clinvar:1; Clinvar (benign):5 |