| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:33440611-33441101 | Common:7; Rare:134 | ||||
| chr5:33441205-33441415 | Common:1; Rare:50 | ||||
| chr5:33891971-33892303 | Rare:78 | ||||
| chr5:34008015-34008334 | Common:2; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656150-34656470 | Common:3; Rare:81 | ||||
| chr5:34915217-34915321 | Rare:30 | ||||
| chr5:34915466-34915766 | Common:1; Rare:84 | ||||
| chr5:34929668-34929908 | Rare:82 | ||||
| chr5:35856803-35856984 | Rare:37 | ||||
| chr5:36151790-36152173 | Rare:100 | ||||
| chr5:36606436-36606680 | Rare:43 | ||||
| chr5:36876630-36876922 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877091-36877155 | Rare:28; Clinvar:1 | ||||
| chr5:37371031-37371375 | Common:2; Rare:89 | ||||
| chr5:37379152-37379392 | Common:1; Rare:67 |