| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:124289-124544 | Common:6; Rare:71 | ||||
| chr4:337609-337857 | Rare:70 | ||||
| chr4:474107-474357 | Common:2; Rare:88 | ||||
| chr4:499124-499285 | Common:3; Rare:59 | ||||
| chr4:673259-673659 | Common:2; Rare:250 | ||||
| chr4:673694-674094 | Common:1; Rare:151 | ||||
| chr4:674243-674570 | Common:2; Rare:153 | ||||
| chr4:681000-681574 | Common:1; Rare:329 | ||||
| chr4:705545-705834 | Common:1; Rare:100 | ||||
| chr4:932220-932523 | Common:2; Rare:122 | ||||
| chr4:973230-973790 | Common:11; Rare:165 | ||||
| chr4:986901-987024 | Common:1; Rare:35; Clinvar:1 | ||||
| chr4:987180-987530 | Common:1; Rare:94; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr4:1011298-1011649 | Common:4; Rare:87 | ||||
| chr4:1233103-1233503 | Rare:151 |