| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88823169-88823388 | Common:2; Rare:40 | ||||
| chr4:89111301-89111621 | Common:4; Rare:120 | ||||
| chr4:89836908-89837253 | Common:3; Rare:110; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:94451735-94451995 | Common:3; Rare:88 | ||||
| chr4:98143450-98143625 | Common:1; Rare:41 | ||||
| chr4:98261153-98261550 | Common:1; Rare:132 | ||||
| chr4:98657637-98657830 | Rare:39 | ||||
| chr4:98929101-98929250 | Common:3; Rare:44 | ||||
| chr4:98995319-98995748 | Common:6; Rare:149 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99563593-99563764 | Common:2; Rare:49 | ||||
| chr4:99563989-99564140 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894357-99894579 | Common:1; Rare:85 | ||||
| chr4:99950228-99950534 | Rare:72 | ||||
| chr4:101347519-101347840 | Common:5; Rare:97 |