| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:84966866-84967030 | Rare:44 | ||||
| chr4:85827651-85827953 | Common:1; Rare:44 | ||||
| chr4:86359837-86360195 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:86594044-86594345 | Rare:97 | ||||
| chr4:86934718-86935088 | Common:2; Rare:125 | ||||
| chr4:87422488-87422823 | Common:2; Rare:89 | ||||
| chr4:88283868-88283890 | Rare:4 | ||||
| chr4:88284246-88284582 | Common:3; Rare:63 | ||||
| chr4:88284584-88284953 | Common:2; Rare:95 | ||||
| chr4:88523591-88523864 | Common:2; Rare:92 | ||||
| chr4:88592276-88592535 | Common:1; Rare:78 | ||||
| chr4:88697741-88697943 | Common:2; Rare:70 | ||||
| chr4:88823148-88823388 | Common:2; Rare:40 | ||||
| chr4:89836148-89836385 | Common:4; Rare:50 | ||||
| chr4:89836866-89837549 | Common:5; Rare:201; Clinvar:5; Clinvar (benign):1 |