| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41560903-41561133 | Common:9; Rare:66 | ||||
| chr22:41589764-41589974 | Common:4; Rare:98 | ||||
| chr22:41621000-41621500 | Common:7; Rare:171 | ||||
| chr22:41621690-41622055 | Common:1; Rare:100 | ||||
| chr22:41800517-41800702 | Common:1; Rare:58 | ||||
| chr22:41832828-41833770 | Common:6; Rare:310 | ||||
| chr22:41976450-41976582 | Rare:25 | ||||
| chr22:41976654-41977073 | Rare:112 | ||||
| chr22:42070770-42071049 | Common:3; Rare:64 | ||||
| chr22:42079616-42079853 | Common:1; Rare:86 | ||||
| chr22:42079940-42080147 | Rare:58 | ||||
| chr22:42090651-42091054 | Common:2; Rare:165; Clinvar (pathogenic):1 | ||||
| chr22:42210684-42210926 | Rare:76 | ||||
| chr22:42343508-42343744 | Rare:76 | ||||
| chr22:42519610-42519965 | Common:2; Rare:138 |