| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39528184-39528307 | Common:2; Rare:30 | ||||
| chr4:39638166-39638348 | Common:1; Rare:32 | ||||
| chr4:39638850-39639229 | Common:1; Rare:147 | ||||
| chr4:39698066-39698370 | Common:1; Rare:94 | ||||
| chr4:39977796-39978070 | Common:2; Rare:84 | ||||
| chr4:40056262-40056568 | Common:3; Rare:72 | ||||
| chr4:40056644-40056984 | Common:4; Rare:103 | ||||
| chr4:40193748-40194148 | Common:4; Rare:85 | ||||
| chr4:40629400-40629750 | Common:1; Rare:61 | ||||
| chr4:40856489-40856889 | Common:4; Rare:133 | ||||
| chr4:40857110-40857302 | Common:2; Rare:69 | ||||
| chr4:41214457-41214580 | Common:2; Rare:33 | ||||
| chr4:41216270-41216750 | Common:6; Rare:134 | ||||
| chr4:41256706-41256954 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:41360532-41360843 | Common:2; Rare:94 |