| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:44024196-44024351 | Common:1; Rare:57 | ||||
| chr22:44498208-44498475 | Common:2; Rare:111 | ||||
| chr22:44668458-44668751 | Common:4; Rare:109 | ||||
| chr22:44752511-44752622 | Common:2; Rare:44 | ||||
| chr22:45163665-45164023 | Common:4; Rare:131 | ||||
| chr22:45309703-45309964 | Common:1; Rare:104 | ||||
| chr22:45413618-45413742 | Rare:42 | ||||
| chr22:45672001-45672076 | Rare:36 | ||||
| chr22:46053778-46053901 | Rare:43 | ||||
| chr22:46150320-46150629 | Common:1; Rare:104 | ||||
| chr22:46250260-46250432 | Common:3; Rare:56 | ||||
| chr22:46267787-46268048 | Common:1; Rare:73 | ||||
| chr22:46296760-46296918 | Rare:53 | ||||
| chr22:46335621-46335797 | Common:5; Rare:80; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46377591-46377860 | Common:6; Rare:66 |