| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19941721-19941879 | Rare:67; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20020897-20021134 | Common:1; Rare:77 | ||||
| chr22:20117290-20117655 | Common:3; Rare:112 | ||||
| chr22:20319999-20320158 | Common:1; Rare:53 | ||||
| chr22:20858971-20859093 | Common:3; Rare:74; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:20982223-20982322 | Common:1; Rare:18; Clinvar (benign):1 | ||||
| chr22:21002092-21002215 | Common:3; Rare:47 | ||||
| chr22:21642034-21642353 | Common:2; Rare:98 | ||||
| chr22:21665934-21666059 | Rare:34 | ||||
| chr22:23894277-23894551 | Common:3; Rare:99 | ||||
| chr22:23894576-23894789 | Common:3; Rare:80 | ||||
| chr22:24555890-24556050 | Rare:49 | ||||
| chr22:26483768-26484046 | Common:9; Rare:134; Clinvar:5; Clinvar (benign):2 | ||||
| chr22:26512428-26512550 | Common:1; Rare:55 | ||||
| chr22:27919204-27919504 | Common:5; Rare:132 |