| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:44678369-44678750 | Common:1; Rare:143 | ||||
| chr4:44726487-44726671 | Common:2; Rare:70 | ||||
| chr4:47463608-47463804 | Common:2; Rare:75 | ||||
| chr4:47485157-47485397 | Common:2; Rare:80 | ||||
| chr4:47914500-47914843 | Common:1; Rare:103 | ||||
| chr4:48341243-48341581 | Common:2; Rare:138 | ||||
| chr4:48483014-48483160 | Common:1; Rare:27 | ||||
| chr4:48780147-48780578 | Common:3; Rare:133 | ||||
| chr4:48830874-48831376 | Common:1; Rare:133 | ||||
| chr4:48831642-48831748 | Rare:18 | ||||
| chr4:51842707-51843248 | Common:3; Rare:157 | ||||
| chr4:52038246-52038431 | Rare:66; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:52862152-52862317 | Common:7; Rare:73 | ||||
| chr4:53365948-53366222 | Rare:60 | ||||
| chr4:53377427-53377722 | Common:3; Rare:86 |