| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98143412-98143662 | Common:1; Rare:64 | ||||
| chr4:98261148-98261519 | Common:1; Rare:123 | ||||
| chr4:98658605-98658913 | Common:2; Rare:86 | ||||
| chr4:98929047-98929388 | Common:3; Rare:98 | ||||
| chr4:98995455-98995823 | Common:6; Rare:129 | ||||
| chr4:99021627-99022342 | Common:2; Rare:120 | ||||
| chr4:99022645-99022809 | Common:1; Rare:39 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99510925-99511059 | Rare:28 | ||||
| chr4:99563593-99563832 | Common:2; Rare:78 | ||||
| chr4:99563948-99564087 | Rare:50 | ||||
| chr4:99564090-99564154 | Common:1; Rare:17; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:99894345-99894625 | Common:3; Rare:96 | ||||
| chr4:99946556-99946799 | Rare:86 | ||||
| chr4:99950172-99950542 | Common:1; Rare:102 |