| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17774382-17774613 | Rare:73 | ||||
| chr22:18077814-18078047 | Common:4; Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19854814-19855106 | Common:1; Rare:114 | ||||
| chr22:19941750-19941886 | Rare:53; Clinvar:4 | ||||
| chr22:20117212-20117557 | Common:3; Rare:108 | ||||
| chr22:20495803-20496002 | Common:2; Rare:72 | ||||
| chr22:20858780-20859093 | Common:4; Rare:155; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:20964894-20965189 | Common:2; Rare:72 | ||||
| chr22:20982200-20982342 | Common:2; Rare:31; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:24555014-24555437 | Common:4; Rare:154 | ||||
| chr22:24555821-24556012 | Rare:56 | ||||
| chr22:25564752-25565050 | Common:1; Rare:129 | ||||
| chr22:26483791-26484074 | Common:9; Rare:124; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:26512442-26512649 | Common:2; Rare:84 | ||||
| chr22:26590076-26590220 | Common:3; Rare:59 |