| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:51844673-51844932 | Common:1; Rare:73 | ||||
| chr4:52038246-52038331 | Rare:35; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:52051288-52051631 | Common:1; Rare:90 | ||||
| chr4:52659146-52659439 | Common:1; Rare:95 | ||||
| chr4:52862152-52862336 | Common:7; Rare:81 | ||||
| chr4:53365349-53365473 | Common:1; Rare:33 | ||||
| chr4:53365953-53366100 | Rare:29 | ||||
| chr4:53377532-53377920 | Common:2; Rare:129 | ||||
| chr4:53377941-53378176 | Common:2; Rare:72 | ||||
| chr4:54064473-54064835 | Common:5; Rare:124 | ||||
| chr4:54228937-54229357 | Common:1; Rare:86; Clinvar (benign):4 | ||||
| chr4:54657815-54658075 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):4 | ||||
| chr4:55125583-55125739 | Common:2; Rare:41 | ||||
| chr4:55395840-55395972 | Common:1; Rare:35; Clinvar:2 | ||||
| chr4:55545847-55546058 | Common:2; Rare:53 |