| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:153788615-153788857 | Common:4; Rare:91 | ||||
| chr4:153789081-153789205 | Rare:21 | ||||
| chr4:154491780-154491971 | Common:1; Rare:41 | ||||
| chr4:154550372-154550498 | Rare:38 | ||||
| chr4:156970958-156971184 | Rare:34 | ||||
| chr4:158173023-158173204 | Rare:27 | ||||
| chr4:158671825-158672359 | Common:5; Rare:135; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723348-158723463 | Rare:50 | ||||
| chr4:168092599-168092717 | Rare:21 | ||||
| chr4:168480485-168480639 | Rare:20 | ||||
| chr4:169010227-169010456 | Common:1; Rare:67 | ||||
| chr4:169620381-169620723 | Common:2; Rare:117 | ||||
| chr4:173334280-173334740 | Rare:117 | ||||
| chr4:173530168-173530462 | Common:2; Rare:66 | ||||
| chr4:174283618-174283965 | Common:1; Rare:69 |