| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88284540-88284705 | Common:1; Rare:31 | ||||
| chr4:88523622-88523848 | Common:2; Rare:77 | ||||
| chr4:88592283-88592535 | Common:1; Rare:76 | ||||
| chr4:89836913-89837253 | Common:3; Rare:109; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:92304427-92304637 | Common:1; Rare:28 | ||||
| chr4:94451703-94451995 | Common:4; Rare:95 | ||||
| chr4:95548912-95549149 | Common:2; Rare:50 | ||||
| chr4:95549196-95549303 | Common:1; Rare:18 | ||||
| chr4:98261153-98261499 | Common:1; Rare:107 | ||||
| chr4:98658609-98658905 | Common:2; Rare:79 | ||||
| chr4:98929093-98929216 | Common:3; Rare:39 | ||||
| chr4:99088696-99088900 | Common:7; Rare:93 | ||||
| chr4:99563974-99564165 | Common:2; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894333-99894618 | Common:3; Rare:98 | ||||
| chr4:99950261-99950493 | Rare:42 |