| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:46909190-46909410 | Common:4; Rare:61 | ||||
| chr4:48780245-48780614 | Common:2; Rare:111 | ||||
| chr4:52038246-52038346 | Rare:39; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:55546816-55547011 | Common:2; Rare:68 | ||||
| chr4:56387423-56387545 | Rare:43 | ||||
| chr4:56435470-56435770 | Common:5; Rare:108 | ||||
| chr4:56436045-56436315 | Rare:101 | ||||
| chr4:56467561-56467670 | Common:2; Rare:47; Clinvar (benign):4 | ||||
| chr4:67701117-67701358 | Common:4; Rare:114 | ||||
| chr4:68349952-68350198 | Rare:89 | ||||
| chr4:70902206-70902382 | Common:4; Rare:65 | ||||
| chr4:70993336-70993801 | Common:6; Rare:134 | ||||
| chr4:75514279-75514498 | Rare:74 | ||||
| chr4:75724412-75724713 | Common:1; Rare:87 | ||||
| chr4:75990912-75991046 | Common:1; Rare:48 |