| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48269711-48270110 | Common:8; Rare:260 | ||||
| chr4:48340985-48341758 | Common:10; Rare:684 | ||||
| chr4:48779440-48779840 | Common:6; Rare:236 | ||||
| chr4:48780098-48780674 | Common:10; Rare:459 | ||||
| chr4:48830878-48831422 | Common:3; Rare:340 | ||||
| chr4:48831400-48832245 | Common:3; Rare:284 | ||||
| chr4:48906671-48906920 | Rare:135 | ||||
| chr4:51842716-51843267 | Common:4; Rare:422 | ||||
| chr4:51843330-51843575 | Rare:150 | ||||
| chr4:51844620-51845040 | Common:2; Rare:153 | ||||
| chr4:52038218-52038412 | Rare:151; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):6 | ||||
| chr4:52051060-52051600 | Common:3; Rare:172 | ||||
| chr4:52051874-52052043 | Common:5; Rare:79 | ||||
| chr4:52658322-52659021 | Common:4; Rare:226 | ||||
| chr4:52659136-52659593 | Common:3; Rare:358 |