| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139453747-139454210 | Common:3; Rare:127; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:140373384-140373701 | Common:2; Rare:129 | ||||
| chr4:140523929-140524226 | Common:2; Rare:91 | ||||
| chr4:143184851-143184985 | Common:5; Rare:51 | ||||
| chr4:143336562-143336893 | Rare:75 | ||||
| chr4:143337122-143337191 | Rare:32 | ||||
| chr4:143513349-143513569 | Common:2; Rare:76 | ||||
| chr4:145098141-145098348 | Rare:72 | ||||
| chr4:145482836-145483003 | Rare:28 | ||||
| chr4:145545904-145546061 | Rare:28 | ||||
| chr4:145619081-145619406 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:146522333-146522449 | Common:2; Rare:48 | ||||
| chr4:147617235-147617426 | Common:1; Rare:42 | ||||
| chr4:147684105-147684308 | Common:1; Rare:87 | ||||
| chr4:148442350-148442712 | Rare:104; Clinvar:4; Clinvar (benign):3 |