| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132556836-132557012 | Common:1; Rare:62; Clinvar:1 | ||||
| chr5:132830617-132830775 | Rare:44 | ||||
| chr5:132866422-132866694 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963489-132963840 | Common:1; Rare:87 | ||||
| chr5:132963897-132964006 | Rare:38 | ||||
| chr5:133026504-133026624 | Common:1; Rare:46 | ||||
| chr5:133051851-133052344 | Common:1; Rare:159 | ||||
| chr5:133968551-133968747 | Rare:80 | ||||
| chr5:133980896-133981097 | Common:1; Rare:36 | ||||
| chr5:134004504-134004869 | Common:2; Rare:124 | ||||
| chr5:134004905-134005070 | Rare:33 | ||||
| chr5:134225513-134225631 | Common:1; Rare:44 | ||||
| chr5:134226002-134226437 | Common:1; Rare:142 | ||||
| chr5:134371018-134371194 | Common:1; Rare:48 | ||||
| chr5:134371380-134371623 | Common:3; Rare:109 |