| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:109730057-109730229 | Common:2; Rare:40 | ||||
| chr4:109815380-109815553 | Common:1; Rare:46 | ||||
| chr4:110618624-110618817 | Common:1; Rare:44; Clinvar (pathogenic):1 | ||||
| chr4:110623067-110623131 | Rare:12 | ||||
| chr4:110641966-110642153 | Rare:41 | ||||
| chr4:110642163-110642181 | Rare:3 | ||||
| chr4:112636888-112637226 | Common:2; Rare:93 | ||||
| chr4:112637390-112637570 | Common:3; Rare:47 | ||||
| chr4:112817984-112818245 | Rare:41 | ||||
| chr4:113761135-113761286 | Common:1; Rare:34 | ||||
| chr4:113979576-113979729 | Common:1; Rare:37 | ||||
| chr4:117085505-117085611 | Common:1; Rare:29 | ||||
| chr4:118685245-118685475 | Common:3; Rare:75 | ||||
| chr4:118835952-118836227 | Common:1; Rare:63 | ||||
| chr4:119212355-119212755 | Common:4; Rare:124 |