| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48341243-48341560 | Common:2; Rare:128 | ||||
| chr4:48830856-48831258 | Common:1; Rare:120 | ||||
| chr4:48831656-48831916 | Rare:52 | ||||
| chr4:51842804-51843245 | Common:1; Rare:131 | ||||
| chr4:51843369-51843545 | Rare:59 | ||||
| chr4:52038225-52038402 | Rare:68; Clinvar:10; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr4:52659172-52659446 | Common:1; Rare:93 | ||||
| chr4:52862142-52862336 | Common:7; Rare:87 | ||||
| chr4:53365349-53365473 | Common:1; Rare:33 | ||||
| chr4:53365972-53366211 | Rare:54 | ||||
| chr4:53377539-53377751 | Common:2; Rare:76 | ||||
| chr4:53377874-53377904 | Rare:7 | ||||
| chr4:54064449-54064771 | Common:2; Rare:100 | ||||
| chr4:55346147-55346362 | Common:3; Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55395675-55395958 | Common:6; Rare:91; Clinvar:2 |