| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:128084336-128084734 | Common:2; Rare:142 | ||||
| chr5:131170686-131171002 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chr5:131263909-131264103 | Rare:70 | ||||
| chr5:131635081-131635430 | Common:1; Rare:122 | ||||
| chr5:131796948-131797215 | Rare:75 | ||||
| chr5:132257475-132257744 | Common:8; Rare:72 | ||||
| chr5:132369595-132369785 | Common:4; Rare:56; Clinvar (benign):1 | ||||
| chr5:132410603-132410929 | Common:1; Rare:63 | ||||
| chr5:132490773-132491051 | Rare:71 | ||||
| chr5:132556892-132557045 | Rare:61; Clinvar:1 | ||||
| chr5:132737492-132737608 | Rare:39 | ||||
| chr5:132866467-132866688 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963554-132964006 | Common:2; Rare:134 | ||||
| chr5:133051862-133052355 | Common:1; Rare:156 | ||||
| chr5:133968491-133968815 | Common:1; Rare:130 |