| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:127517529-127517699 | Common:4; Rare:77 | ||||
| chr5:129094465-129094769 | Common:3; Rare:124 | ||||
| chr5:131165194-131165374 | Common:1; Rare:71; Clinvar (benign):1 | ||||
| chr5:131170678-131170996 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr5:131635183-131635484 | Common:1; Rare:113 | ||||
| chr5:131796970-131797213 | Rare:67 | ||||
| chr5:132410772-132410920 | Rare:29 | ||||
| chr5:132490770-132490989 | Rare:51 | ||||
| chr5:132866447-132866688 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133051859-133052107 | Rare:93 | ||||
| chr5:133968560-133968737 | Rare:72 | ||||
| chr5:134004636-134004861 | Common:1; Rare:84 | ||||
| chr5:134004909-134005010 | Rare:22 | ||||
| chr5:134226007-134226407 | Common:1; Rare:130 | ||||
| chr5:134371031-134371184 | Common:1; Rare:39 |