| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88523629-88523848 | Common:2; Rare:76 | ||||
| chr4:88592305-88592535 | Common:1; Rare:70 | ||||
| chr4:94451697-94451998 | Common:4; Rare:97 | ||||
| chr4:98261192-98261499 | Common:1; Rare:95 | ||||
| chr4:98929108-98929385 | Common:3; Rare:68 | ||||
| chr4:99088702-99088884 | Common:6; Rare:79 | ||||
| chr4:99563955-99564170 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894347-99894620 | Common:3; Rare:95 | ||||
| chr4:99950242-99950475 | Rare:49 | ||||
| chr4:101347567-101347834 | Common:4; Rare:81 | ||||
| chr4:102760908-102761084 | Rare:62; Clinvar:1 | ||||
| chr4:102826725-102826988 | Rare:74 | ||||
| chr4:102827148-102827228 | Rare:26 | ||||
| chr4:102827439-102827960 | Common:4; Rare:171 | ||||
| chr4:102827963-102827987 | Rare:5 |