| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:41934935-41935256 | Common:3; Rare:87 | ||||
| chr4:41990402-41990580 | Common:1; Rare:65 | ||||
| chr4:44678369-44678731 | Common:1; Rare:137 | ||||
| chr4:44726498-44726642 | Common:1; Rare:51 | ||||
| chr4:47485166-47485372 | Common:1; Rare:68 | ||||
| chr4:48016624-48016794 | Common:1; Rare:50 | ||||
| chr4:48017197-48017491 | Common:2; Rare:56 | ||||
| chr4:48269802-48269981 | Common:1; Rare:37 | ||||
| chr4:48341253-48341581 | Common:1; Rare:134 | ||||
| chr4:48780147-48780572 | Common:3; Rare:131 | ||||
| chr4:51842779-51843224 | Common:1; Rare:130 | ||||
| chr4:51843416-51843715 | Rare:75 | ||||
| chr4:52038233-52038329 | Rare:43; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:52659193-52659439 | Common:1; Rare:82 | ||||
| chr4:53365953-53366222 | Rare:60 |