| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:87422488-87422691 | Common:1; Rare:62 | ||||
| chr4:87422828-87422899 | Rare:29 | ||||
| chr4:88284223-88284261 | Rare:9 | ||||
| chr4:88284408-88284966 | Common:4; Rare:131 | ||||
| chr4:88378881-88379096 | Common:3; Rare:74 | ||||
| chr4:88523591-88523875 | Common:2; Rare:94 | ||||
| chr4:88592277-88592520 | Common:1; Rare:72 | ||||
| chr4:88697791-88697979 | Common:2; Rare:48 | ||||
| chr4:88823130-88823467 | Common:3; Rare:62 | ||||
| chr4:89057122-89057282 | Common:1; Rare:35 | ||||
| chr4:89111410-89111651 | Common:2; Rare:80 | ||||
| chr4:89111745-89111838 | Rare:27 | ||||
| chr4:89836882-89837566 | Common:5; Rare:205; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:94207843-94208023 | Common:1; Rare:62 | ||||
| chr4:94451694-94452039 | Common:4; Rare:110 |