| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:47914486-47914843 | Common:1; Rare:109 | ||||
| chr4:48016634-48016774 | Common:1; Rare:38 | ||||
| chr4:48269831-48269971 | Common:1; Rare:26 | ||||
| chr4:48341251-48341581 | Common:2; Rare:134 | ||||
| chr4:48830844-48831411 | Common:1; Rare:155 | ||||
| chr4:51843340-51843545 | Rare:66 | ||||
| chr4:52038237-52038346 | Rare:46; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:52659177-52659422 | Common:1; Rare:84 | ||||
| chr4:52862119-52862322 | Common:7; Rare:95 | ||||
| chr4:53365997-53366153 | Rare:32 | ||||
| chr4:53377555-53377773 | Common:2; Rare:78 | ||||
| chr4:53558011-53558313 | Common:3; Rare:57 | ||||
| chr4:54657822-54658021 | Common:2; Rare:76; Clinvar (benign):1 | ||||
| chr4:55346191-55346347 | Common:3; Rare:54; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55546490-55546545 | Rare:13 |