| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20080087-20080301 | Rare:78 | ||||
| chr22:20116886-20117656 | Common:5; Rare:231 | ||||
| chr22:20319882-20320158 | Common:2; Rare:102 | ||||
| chr22:20495765-20496010 | Common:2; Rare:88 | ||||
| chr22:20507458-20507718 | Rare:93 | ||||
| chr22:20507927-20508076 | Rare:34 | ||||
| chr22:20858639-20859121 | Common:9; Rare:242; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr22:20917182-20917495 | Rare:118 | ||||
| chr22:20982204-20982407 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr22:21642106-21642331 | Common:2; Rare:66 | ||||
| chr22:21652022-21652193 | Common:1; Rare:40 | ||||
| chr22:21867635-21867794 | Common:1; Rare:40 | ||||
| chr22:22558980-22559374 | Common:1; Rare:125 | ||||
| chr22:23145243-23145515 | Common:2; Rare:98 | ||||
| chr22:23751117-23751146 | Common:1; Rare:11 |