| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:129094468-129094760 | Common:3; Rare:118 | ||||
| chr5:131170678-131171008 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr5:131635160-131635393 | Common:1; Rare:91 | ||||
| chr5:131796940-131797234 | Rare:82 | ||||
| chr5:132556836-132557039 | Common:1; Rare:74; Clinvar:1 | ||||
| chr5:132737485-132737698 | Rare:69 | ||||
| chr5:132866486-132866694 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133051851-133052216 | Rare:125 | ||||
| chr5:133968565-133968718 | Rare:64 | ||||
| chr5:134004535-134004999 | Common:1; Rare:144 | ||||
| chr5:134371027-134371184 | Common:1; Rare:40 | ||||
| chr5:134411843-134412002 | Rare:52 | ||||
| chr5:134648689-134648816 | Rare:37 | ||||
| chr5:134845843-134846094 | Rare:114 | ||||
| chr5:134874250-134874418 | Common:1; Rare:85 |