| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177554373-177554617 | Common:8; Rare:78 | ||||
| chr5:177591937-177592252 | Common:1; Rare:100 | ||||
| chr5:177600021-177600155 | Common:3; Rare:42 | ||||
| chr5:178130868-178131109 | Common:1; Rare:63 | ||||
| chr5:178153719-178154246 | Rare:144; Clinvar:6; Clinvar (benign):2 | ||||
| chr5:178204358-178204631 | Common:4; Rare:112 | ||||
| chr5:178626940-178627156 | Rare:57 | ||||
| chr5:179550323-179550561 | Common:4; Rare:68 | ||||
| chr5:179550797-179550876 | Rare:31 | ||||
| chr5:179559536-179559814 | Common:1; Rare:78 | ||||
| chr5:179607351-179607652 | Common:1; Rare:95 | ||||
| chr5:179623596-179623948 | Common:4; Rare:131 | ||||
| chr5:179698575-179699091 | Common:4; Rare:182 | ||||
| chr5:179726574-179726739 | Rare:41 | ||||
| chr5:179806310-179806449 | Rare:44 |