| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:53377434-53377729 | Common:3; Rare:88 | ||||
| chr4:54064558-54064838 | Common:4; Rare:100 | ||||
| chr4:55346175-55346321 | Common:3; Rare:47; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:55948703-55948840 | Rare:28 | ||||
| chr4:56387423-56387553 | Rare:44 | ||||
| chr4:56435475-56435759 | Common:5; Rare:103 | ||||
| chr4:56436048-56436307 | Rare:96 | ||||
| chr4:56467527-56467633 | Rare:44 | ||||
| chr4:56977574-56977785 | Common:1; Rare:81 | ||||
| chr4:67545442-67545742 | Common:2; Rare:76 | ||||
| chr4:67701097-67701371 | Common:4; Rare:130 | ||||
| chr4:68349975-68350209 | Common:1; Rare:85 | ||||
| chr4:70688454-70688568 | Common:2; Rare:31 | ||||
| chr4:70902189-70902363 | Common:4; Rare:65 | ||||
| chr4:70993321-70993815 | Common:6; Rare:142 |