| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:87007097-87007254 | Common:1; Rare:49 | ||||
| chr4:87391125-87391499 | Common:4; Rare:103 | ||||
| chr4:87422559-87422830 | Common:1; Rare:66 | ||||
| chr4:88523590-88523882 | Common:2; Rare:97 | ||||
| chr4:88592300-88592529 | Common:1; Rare:69 | ||||
| chr4:88823168-88823477 | Common:2; Rare:60 | ||||
| chr4:89057127-89057273 | Common:1; Rare:32 | ||||
| chr4:89111406-89111644 | Common:2; Rare:80 | ||||
| chr4:89836975-89837569 | Common:5; Rare:177; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:94207843-94207942 | Rare:40 | ||||
| chr4:94451745-94451979 | Common:3; Rare:78 | ||||
| chr4:98261135-98261519 | Common:2; Rare:129 | ||||
| chr4:98929101-98929378 | Common:3; Rare:70 | ||||
| chr4:98995468-98995763 | Common:6; Rare:105 | ||||
| chr4:99088704-99088879 | Common:6; Rare:75 |