| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20116966-20117016 | Common:1; Rare:10 | ||||
| chr22:20117175-20117571 | Common:3; Rare:127 | ||||
| chr22:20319984-20320160 | Common:2; Rare:62 | ||||
| chr22:20495771-20495985 | Common:2; Rare:79 | ||||
| chr22:20858684-20859105 | Common:7; Rare:208; Clinvar:3; Clinvar (benign):4 | ||||
| chr22:20982191-20982353 | Common:2; Rare:39; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002061-21002262 | Common:5; Rare:80 | ||||
| chr22:21642023-21642366 | Common:2; Rare:106 | ||||
| chr22:21937974-21938365 | Rare:111 | ||||
| chr22:23857580-23857916 | Common:5; Rare:129 | ||||
| chr22:23894311-23894695 | Common:6; Rare:150 | ||||
| chr22:23895118-23895353 | Common:2; Rare:95 | ||||
| chr22:24245043-24245306 | Common:2; Rare:46 | ||||
| chr22:24270780-24271174 | Common:5; Rare:155 | ||||
| chr22:24555005-24555437 | Common:4; Rare:157 |