| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23786821-23787101 | Common:3; Rare:97; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:23838992-23839044 | Rare:23 | ||||
| chr22:23894318-23894919 | Common:6; Rare:241; Clinvar:1 | ||||
| chr22:24244498-24244585 | Rare:30 | ||||
| chr22:24245053-24245282 | Common:2; Rare:40 | ||||
| chr22:24271080-24271174 | Common:1; Rare:47 | ||||
| chr22:24554972-24555412 | Common:4; Rare:159 | ||||
| chr22:24555829-24556065 | Rare:72 | ||||
| chr22:24592940-24593114 | Common:3; Rare:53 | ||||
| chr22:26472412-26472678 | Common:3; Rare:65 | ||||
| chr22:26483752-26483964 | Common:4; Rare:91; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512413-26512561 | Common:1; Rare:64 | ||||
| chr22:26590077-26590220 | Common:3; Rare:58 | ||||
| chr22:27801716-27801756 | Rare:18 | ||||
| chr22:27918842-27918891 | Rare:11 |