| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20116961-20117621 | Common:4; Rare:195 | ||||
| chr22:20319999-20320114 | Common:1; Rare:45 | ||||
| chr22:20495771-20495904 | Common:1; Rare:48 | ||||
| chr22:20507922-20508070 | Rare:34 | ||||
| chr22:20508506-20508556 | Rare:11 | ||||
| chr22:20582874-20583174 | Rare:90 | ||||
| chr22:20858840-20859100 | Common:4; Rare:134; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:20917238-20917490 | Rare:93 | ||||
| chr22:20981692-20981999 | Common:1; Rare:76 | ||||
| chr22:20982191-20982358 | Common:2; Rare:40; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002088-21002289 | Common:6; Rare:74 | ||||
| chr22:21032541-21032646 | Rare:43 | ||||
| chr22:21629991-21630286 | Common:3; Rare:94 | ||||
| chr22:21642042-21642405 | Common:2; Rare:114 | ||||
| chr22:21665934-21666070 | Rare:41 |