| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:153344504-153344731 | Common:4; Rare:65 | ||||
| chr4:154541075-154541409 | Common:3; Rare:57 | ||||
| chr4:155353001-155353335 | Common:1; Rare:78 | ||||
| chr4:155953722-155953993 | Rare:83 | ||||
| chr4:156774035-156774165 | Rare:19 | ||||
| chr4:156774437-156774717 | Common:5; Rare:49 | ||||
| chr4:156970928-156971221 | Rare:46 | ||||
| chr4:158172371-158172744 | Rare:63 | ||||
| chr4:158671730-158672166 | Common:5; Rare:124; Clinvar:1 | ||||
| chr4:158672199-158672344 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:158723207-158723295 | Rare:33 | ||||
| chr4:158723306-158723432 | Common:2; Rare:61 | ||||
| chr4:163166393-163166445 | Common:1; Rare:25 | ||||
| chr4:163166860-163166994 | Common:2; Rare:47 | ||||
| chr4:163494444-163494676 | Common:2; Rare:87 |