| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:13545070-13545169 | Rare:20 | ||||
| chr4:13627394-13627568 | Rare:56 | ||||
| chr4:13627675-13627877 | Common:1; Rare:62 | ||||
| chr4:15002165-15002505 | Common:2; Rare:134 | ||||
| chr4:15002956-15002985 | Rare:16 | ||||
| chr4:15003061-15003172 | Rare:59 | ||||
| chr4:15469762-15469906 | Common:1; Rare:28 | ||||
| chr4:15655283-15655477 | Common:1; Rare:85 | ||||
| chr4:15681406-15681898 | Common:4; Rare:163 | ||||
| chr4:17512047-17512252 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr4:17577300-17577567 | Rare:124 | ||||
| chr4:17614540-17614670 | Common:2; Rare:60 | ||||
| chr4:17810598-17811091 | Common:4; Rare:146 | ||||
| chr4:18021701-18021920 | Common:2; Rare:95 | ||||
| chr4:20700313-20700548 | Common:3; Rare:97 |