| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:18024476-18024641 | Common:1; Rare:51 | ||||
| chr22:18077780-18078022 | Common:5; Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19122350-19122661 | Common:5; Rare:83 | ||||
| chr22:19144627-19144920 | Common:5; Rare:105 | ||||
| chr22:19178449-19178540 | Common:1; Rare:24 | ||||
| chr22:19291707-19291917 | Common:9; Rare:64 | ||||
| chr22:19432327-19432587 | Common:2; Rare:106 | ||||
| chr22:19447680-19447972 | Common:2; Rare:116 | ||||
| chr22:19479117-19479473 | Common:4; Rare:128 | ||||
| chr22:19720203-19720453 | Rare:77 | ||||
| chr22:19854795-19855063 | Common:1; Rare:100 | ||||
| chr22:19941715-19941886 | Rare:73; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20020916-20021134 | Common:1; Rare:69 | ||||
| chr22:20079921-20080292 | Common:1; Rare:120 | ||||
| chr22:20117163-20117577 | Common:3; Rare:133 |