| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:18077780-18078022 | Common:5; Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19291707-19291915 | Common:9; Rare:64 | ||||
| chr22:19432294-19432616 | Common:4; Rare:136 | ||||
| chr22:19447667-19447852 | Common:2; Rare:82 | ||||
| chr22:19479107-19479473 | Common:4; Rare:135 | ||||
| chr22:19854795-19854995 | Rare:69 | ||||
| chr22:19941746-19942136 | Common:2; Rare:101; Clinvar:4 | ||||
| chr22:20020892-20021134 | Common:1; Rare:78 | ||||
| chr22:20079921-20080258 | Common:1; Rare:108 | ||||
| chr22:20116975-20117013 | Rare:7 | ||||
| chr22:20117221-20117606 | Common:3; Rare:123 | ||||
| chr22:20319998-20320117 | Common:1; Rare:47 | ||||
| chr22:20495775-20495898 | Common:1; Rare:47 | ||||
| chr22:20858704-20859113 | Common:8; Rare:207; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr22:20982183-20982358 | Common:2; Rare:43; Clinvar (benign):2; Clinvar (pathogenic):1 |