| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:89836122-89836259 | Common:4; Rare:33 | ||||
| chr4:89836819-89837292 | Common:4; Rare:150; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:89837400-89837785 | Rare:79 | ||||
| chr4:89838279-89838352 | Rare:14 | ||||
| chr4:90127227-90127590 | Common:1; Rare:112 | ||||
| chr4:94207557-94207974 | Common:2; Rare:125 | ||||
| chr4:94757754-94758053 | Common:4; Rare:79 | ||||
| chr4:95548992-95549149 | Common:1; Rare:33 | ||||
| chr4:98143450-98143649 | Common:1; Rare:51 | ||||
| chr4:98261136-98261550 | Common:1; Rare:142 | ||||
| chr4:98929101-98929412 | Common:3; Rare:75 | ||||
| chr4:98995493-98995752 | Common:6; Rare:93 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99563604-99563825 | Common:2; Rare:67 | ||||
| chr4:99563969-99564127 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2 |