| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:44726487-44726642 | Common:2; Rare:54 | ||||
| chr4:47463612-47463790 | Common:2; Rare:66 | ||||
| chr4:47485211-47485353 | Common:1; Rare:51 | ||||
| chr4:51843350-51843468 | Rare:50 | ||||
| chr4:54229801-54230064 | Common:2; Rare:50 | ||||
| chr4:55346194-55346337 | Common:3; Rare:50; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55395852-55395957 | Common:1; Rare:28; Clinvar:2 | ||||
| chr4:55546809-55547028 | Common:2; Rare:78 | ||||
| chr4:56387409-56387545 | Rare:47 | ||||
| chr4:56435475-56435973 | Common:6; Rare:163 | ||||
| chr4:56467532-56467656 | Common:1; Rare:50; Clinvar (benign):2 | ||||
| chr4:56977597-56977785 | Common:1; Rare:65 | ||||
| chr4:57110383-57110536 | Common:1; Rare:49 | ||||
| chr4:67545423-67545742 | Common:2; Rare:80 | ||||
| chr4:67701099-67701371 | Common:4; Rare:130 |