| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19854787-19855013 | Rare:83 | ||||
| chr22:19941685-19941886 | Rare:84; Clinvar:6; Clinvar (benign):5 | ||||
| chr22:20020897-20021134 | Common:1; Rare:77 | ||||
| chr22:20079936-20080305 | Common:1; Rare:122 | ||||
| chr22:20117175-20117655 | Common:4; Rare:157 | ||||
| chr22:20319989-20320141 | Common:2; Rare:54 | ||||
| chr22:20394018-20394174 | Rare:50 | ||||
| chr22:20495775-20495920 | Common:1; Rare:55 | ||||
| chr22:20917153-20917431 | Rare:99 | ||||
| chr22:20982191-20982353 | Common:2; Rare:39; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002094-21002223 | Common:3; Rare:46 | ||||
| chr22:21642055-21642353 | Common:2; Rare:89 | ||||
| chr22:21665934-21666083 | Rare:46 | ||||
| chr22:23894307-23894522 | Common:3; Rare:82 | ||||
| chr22:23894524-23894879 | Common:3; Rare:141; Clinvar:1 |