| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:94451789-94451995 | Common:3; Rare:66 | ||||
| chr4:98143454-98143578 | Rare:29 | ||||
| chr4:98261136-98261536 | Common:1; Rare:133 | ||||
| chr4:98657618-98657830 | Rare:41 | ||||
| chr4:98658589-98658919 | Common:2; Rare:95 | ||||
| chr4:98929041-98929397 | Common:3; Rare:103 | ||||
| chr4:98995468-98995771 | Common:6; Rare:109 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99144209-99144490 | Common:3; Rare:43 | ||||
| chr4:99291444-99291558 | Rare:27 | ||||
| chr4:99321311-99321692 | Common:4; Rare:87 | ||||
| chr4:99352989-99353179 | Common:2; Rare:39 | ||||
| chr4:99563593-99563772 | Common:2; Rare:49 | ||||
| chr4:99563935-99564173 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894333-99894595 | Common:2; Rare:94 |