| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:123423313-123423618 | Rare:108 | ||||
| chr5:124746755-124746844 | Common:1; Rare:18 | ||||
| chr5:124748800-124748997 | Common:1; Rare:49 | ||||
| chr5:126423320-126423609 | Rare:84 | ||||
| chr5:126595160-126595327 | Common:2; Rare:83; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr5:127030509-127030768 | Common:2; Rare:62 | ||||
| chr5:127290777-127290844 | Rare:9 | ||||
| chr5:128083583-128083766 | Common:2; Rare:75 | ||||
| chr5:128965413-128965561 | Common:2; Rare:43 | ||||
| chr5:129094474-129094794 | Common:3; Rare:140 | ||||
| chr5:131170705-131171006 | Common:1; Rare:61; Clinvar (benign):2 | ||||
| chr5:131263908-131264117 | Rare:76 | ||||
| chr5:131796926-131797227 | Rare:87 | ||||
| chr5:132257483-132257742 | Common:8; Rare:69 | ||||
| chr5:132369636-132369725 | Common:1; Rare:21 |