| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:47837945-47838158 | Rare:47 | ||||
| chr4:48269807-48270030 | Common:1; Rare:48 | ||||
| chr4:48341214-48341507 | Common:1; Rare:120 | ||||
| chr4:52659172-52659420 | Common:1; Rare:86 | ||||
| chr4:52751601-52751759 | Common:2; Rare:43 | ||||
| chr4:52862180-52862322 | Common:5; Rare:63 | ||||
| chr4:55395838-55395968 | Common:1; Rare:32; Clinvar:2 | ||||
| chr4:56387417-56387528 | Rare:35 | ||||
| chr4:56435484-56435713 | Common:5; Rare:83 | ||||
| chr4:56467542-56467708 | Common:2; Rare:68; Clinvar (benign):5 | ||||
| chr4:56681275-56681380 | Rare:15 | ||||
| chr4:56977574-56977765 | Common:1; Rare:75 | ||||
| chr4:65670455-65670611 | Rare:39 | ||||
| chr4:67545442-67545724 | Common:2; Rare:69 | ||||
| chr4:67701115-67701358 | Common:4; Rare:116 |