| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48780217-48780572 | Common:3; Rare:105 | ||||
| chr4:52038240-52038391 | Rare:59; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:52659204-52659477 | Common:1; Rare:93 | ||||
| chr4:52862095-52862322 | Common:8; Rare:104 | ||||
| chr4:53366003-53366134 | Rare:25 | ||||
| chr4:53377434-53377710 | Common:3; Rare:83 | ||||
| chr4:53558179-53558329 | Common:3; Rare:32 | ||||
| chr4:54228932-54229345 | Common:1; Rare:86; Clinvar (benign):4 | ||||
| chr4:54657818-54658030 | Common:2; Rare:79; Clinvar (benign):2 | ||||
| chr4:55546801-55546982 | Common:2; Rare:63 | ||||
| chr4:56387423-56387524 | Rare:35 | ||||
| chr4:56435481-56435753 | Common:5; Rare:101 | ||||
| chr4:56435975-56436307 | Rare:115 | ||||
| chr4:56467515-56467708 | Common:2; Rare:79; Clinvar (benign):5 | ||||
| chr4:56505459-56505835 | Common:4; Rare:96 |