| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48780217-48780626 | Common:3; Rare:124 | ||||
| chr4:52659234-52659420 | Common:1; Rare:63 | ||||
| chr4:54064424-54064540 | Rare:33 | ||||
| chr4:55948720-55948865 | Rare:29 | ||||
| chr4:56387414-56387516 | Rare:33 | ||||
| chr4:56435473-56435770 | Common:5; Rare:107 | ||||
| chr4:56435965-56436315 | Rare:128 | ||||
| chr4:56467521-56467679 | Common:2; Rare:68; Clinvar (benign):4 | ||||
| chr4:56977597-56977763 | Common:1; Rare:57 | ||||
| chr4:67545455-67545742 | Common:2; Rare:72 | ||||
| chr4:67701115-67701358 | Common:4; Rare:116 | ||||
| chr4:69760521-69760848 | Rare:57 | ||||
| chr4:70688226-70688579 | Common:2; Rare:93 | ||||
| chr4:70902202-70902382 | Common:4; Rare:67 | ||||
| chr4:70993345-70993658 | Common:5; Rare:90 |