| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179559537-179559781 | Common:1; Rare:66 | ||||
| chr5:179623601-179623950 | Common:4; Rare:128 | ||||
| chr5:179698575-179699102 | Common:4; Rare:186 | ||||
| chr5:179806298-179806472 | Rare:60 | ||||
| chr5:179806494-179806570 | Rare:24 | ||||
| chr5:179806817-179807063 | Common:3; Rare:91 | ||||
| chr5:179820731-179820964 | Common:4; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179820967-179821141 | Common:1; Rare:54; Clinvar:8; Clinvar (benign):2 | ||||
| chr5:179823855-179824338 | Common:1; Rare:200; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:179858796-179859047 | Rare:134 | ||||
| chr5:180649571-180649788 | Rare:66 | ||||
| chr5:180802762-180802976 | Common:8; Rare:84 | ||||
| chr5:180810108-180810269 | Common:3; Rare:46 | ||||
| chr5:181040075-181040299 | Rare:46 | ||||
| chr5:181223115-181223328 | Rare:77 |