| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132737485-132737639 | Rare:53 | ||||
| chr5:132777118-132777221 | Common:3; Rare:25 | ||||
| chr5:132866447-132866694 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132873531-132873668 | Common:1; Rare:37 | ||||
| chr5:133051851-133052157 | Rare:109 | ||||
| chr5:133968516-133968700 | Rare:86 | ||||
| chr5:134004647-134004869 | Common:1; Rare:83 | ||||
| chr5:134004913-134004988 | Rare:17 | ||||
| chr5:134176859-134177253 | Common:4; Rare:131 | ||||
| chr5:134371000-134371184 | Common:1; Rare:48 | ||||
| chr5:134411846-134412008 | Rare:56 | ||||
| chr5:134632751-134632918 | Rare:35 | ||||
| chr5:134648682-134648816 | Rare:39 | ||||
| chr5:134874254-134874436 | Common:1; Rare:95 | ||||
| chr5:135578989-135579291 | Common:2; Rare:80 |