| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26860565-26860796 | Common:1; Rare:71 | ||||
| chr4:30720270-30720611 | Common:2; Rare:88 | ||||
| chr4:37826472-37826735 | Common:7; Rare:90 | ||||
| chr4:37977152-37977447 | Rare:78 | ||||
| chr4:38664252-38664301 | Rare:22 | ||||
| chr4:38867668-38867822 | Common:1; Rare:62 | ||||
| chr4:39182202-39182554 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39366319-39366422 | Rare:32 | ||||
| chr4:39458768-39459148 | Common:4; Rare:187; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:39527107-39527305 | Common:2; Rare:42 | ||||
| chr4:39527337-39527789 | Common:4; Rare:121 | ||||
| chr4:39527925-39528029 | Rare:24 | ||||
| chr4:39638829-39639165 | Common:1; Rare:122 | ||||
| chr4:39697911-39698359 | Common:2; Rare:165 | ||||
| chr4:40056601-40056941 | Common:4; Rare:105 |