| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:140756098-140756457 | Common:1; Rare:71 | ||||
| chr4:141220804-141220993 | Rare:69 | ||||
| chr4:142405371-142405599 | Common:1; Rare:38 | ||||
| chr4:142846435-142846633 | Common:1; Rare:38 | ||||
| chr4:143337116-143337220 | Rare:45 | ||||
| chr4:144140673-144140956 | Common:3; Rare:52 | ||||
| chr4:144645854-144646168 | Common:1; Rare:92 | ||||
| chr4:144646371-144646697 | Common:1; Rare:79 | ||||
| chr4:145098107-145098359 | Rare:82 | ||||
| chr4:145180564-145180857 | Common:1; Rare:81 | ||||
| chr4:145481524-145481703 | Rare:44 | ||||
| chr4:145482869-145483001 | Rare:21 | ||||
| chr4:145619327-145619418 | Rare:35; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:145938413-145938737 | Common:2; Rare:59 | ||||
| chr4:145938786-145938973 | Rare:50 |