| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132370147-132370180 | Rare:13; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:132410602-132410995 | Common:1; Rare:81 | ||||
| chr5:132490761-132491020 | Rare:68 | ||||
| chr5:132556813-132557032 | Common:1; Rare:74; Clinvar:1 | ||||
| chr5:132830634-132830775 | Rare:42 | ||||
| chr5:132866318-132866705 | Common:1; Rare:117; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963499-132963746 | Rare:67 | ||||
| chr5:133026519-133026759 | Common:4; Rare:57 | ||||
| chr5:133051862-133052357 | Common:1; Rare:156 | ||||
| chr5:133968573-133968688 | Rare:54 | ||||
| chr5:134004535-134004869 | Common:1; Rare:109 | ||||
| chr5:134004894-134005035 | Rare:31 | ||||
| chr5:134225548-134225591 | Common:1; Rare:13 | ||||
| chr5:134225969-134226407 | Common:1; Rare:142 | ||||
| chr5:134371010-134371199 | Common:1; Rare:50 |