| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34915461-34915752 | Common:1; Rare:75 | ||||
| chr5:35938577-35938842 | Common:1; Rare:50 | ||||
| chr5:36151806-36152195 | Rare:109 | ||||
| chr5:36241565-36241959 | Common:5; Rare:138; Clinvar:1; Clinvar (benign):5 | ||||
| chr5:36242158-36242334 | Common:1; Rare:45 | ||||
| chr5:36876607-36876903 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37249317-37249696 | Common:1; Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:38556472-38556776 | Common:3; Rare:101 | ||||
| chr5:39074346-39074505 | Common:1; Rare:71 | ||||
| chr5:40755832-40756018 | Rare:46 | ||||
| chr5:40798158-40798368 | Common:1; Rare:77 | ||||
| chr5:40834541-40834670 | Common:1; Rare:35 | ||||
| chr5:40835181-40835319 | Common:2; Rare:58 | ||||
| chr5:41870360-41870591 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:41903961-41904239 | Common:1; Rare:68 |