| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37552350-37552750 | Common:2; Rare:118 | ||||
| chr22:37561708-37562108 | Common:1; Rare:166 | ||||
| chr22:37601611-37602011 | Common:4; Rare:117 | ||||
| chr22:37633636-37633794 | Common:1; Rare:39 | ||||
| chr22:37802332-37802560 | Common:2; Rare:61 | ||||
| chr22:37803704-37803876 | Rare:33 | ||||
| chr22:37817650-37818020 | Common:4; Rare:97 | ||||
| chr22:37818114-37818586 | Common:3; Rare:177 | ||||
| chr22:38016439-38016839 | Rare:85; Clinvar (pathogenic):1 | ||||
| chr22:38034351-38034851 | Common:2; Rare:120 | ||||
| chr22:38052332-38052732 | Common:1; Rare:97 | ||||
| chr22:38097685-38098085 | Common:1; Rare:115 | ||||
| chr22:38177870-38178200 | Common:3; Rare:50 | ||||
| chr22:38214698-38215098 | Common:2; Rare:165 | ||||
| chr22:38397176-38397576 | Common:4; Rare:173 |