| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132866394-132866694 | Common:1; Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133051862-133052136 | Rare:100 | ||||
| chr5:133968563-133968722 | Rare:66 | ||||
| chr5:134004654-134004838 | Common:1; Rare:70 | ||||
| chr5:134004916-134005003 | Rare:20 | ||||
| chr5:134371031-134371184 | Common:1; Rare:39 | ||||
| chr5:134411850-134411948 | Rare:37 | ||||
| chr5:134632773-134632937 | Rare:32 | ||||
| chr5:134738423-134738573 | Rare:53 | ||||
| chr5:134845843-134846089 | Rare:112 | ||||
| chr5:134874261-134874411 | Common:1; Rare:77 | ||||
| chr5:136028821-136029187 | Rare:108; Clinvar:2 | ||||
| chr5:137754332-137754505 | Rare:52 | ||||
| chr5:138178620-138178707 | Rare:25 | ||||
| chr5:138178943-138179190 | Common:3; Rare:51 |