| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:47463629-47463790 | Common:2; Rare:56 | ||||
| chr4:47485204-47485340 | Common:1; Rare:52 | ||||
| chr4:48341266-48341483 | Rare:88 | ||||
| chr4:48780197-48780651 | Common:4; Rare:141 | ||||
| chr4:48830844-48831223 | Common:1; Rare:120 | ||||
| chr4:52038231-52038580 | Common:1; Rare:111; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:52659188-52659422 | Common:1; Rare:80 | ||||
| chr4:53365349-53365446 | Common:1; Rare:26 | ||||
| chr4:53377434-53377824 | Common:4; Rare:120 | ||||
| chr4:53558179-53558314 | Common:3; Rare:29 | ||||
| chr4:54229002-54229345 | Common:1; Rare:77; Clinvar (benign):4 | ||||
| chr4:54657714-54658030 | Common:3; Rare:120; Clinvar (benign):2 | ||||
| chr4:55546801-55547003 | Common:2; Rare:70 | ||||
| chr4:55636188-55636422 | Common:1; Rare:69 | ||||
| chr4:55948766-55948964 | Common:1; Rare:38 |