| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:87422492-87422647 | Common:1; Rare:47 | ||||
| chr4:88592305-88592491 | Common:1; Rare:49 | ||||
| chr4:88823126-88823338 | Common:3; Rare:36 | ||||
| chr4:89057150-89057258 | Rare:25 | ||||
| chr4:89111332-89111581 | Common:4; Rare:94 | ||||
| chr4:89836971-89837528 | Common:5; Rare:166; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:94207843-94207940 | Rare:38 | ||||
| chr4:94451702-94451982 | Common:4; Rare:90 | ||||
| chr4:95548960-95549114 | Common:1; Rare:36 | ||||
| chr4:98261136-98261519 | Common:1; Rare:129 | ||||
| chr4:98658609-98658890 | Common:2; Rare:78 | ||||
| chr4:98929031-98929385 | Common:3; Rare:103 | ||||
| chr4:98995502-98995783 | Common:5; Rare:97 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99563591-99563775 | Common:2; Rare:51 |