| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:92304165-92304307 | Rare:45 | ||||
| chr4:94207518-94207724 | Common:2; Rare:59 | ||||
| chr4:94451792-94452002 | Common:3; Rare:65 | ||||
| chr4:94757711-94758046 | Common:4; Rare:97 | ||||
| chr4:95548814-95548882 | Rare:34 | ||||
| chr4:95549000-95549359 | Common:2; Rare:75 | ||||
| chr4:98143474-98143638 | Common:1; Rare:41 | ||||
| chr4:98261136-98261566 | Common:1; Rare:149 | ||||
| chr4:98657637-98657790 | Rare:32 | ||||
| chr4:98929101-98929203 | Common:3; Rare:30 | ||||
| chr4:98995390-98995773 | Common:6; Rare:133 | ||||
| chr4:99088696-99088884 | Common:6; Rare:85 | ||||
| chr4:99563922-99564165 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894333-99894620 | Common:3; Rare:98 | ||||
| chr4:99946551-99946985 | Common:1; Rare:140 |