| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:178153775-178154110 | Rare:101; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178859881-178860096 | Common:3; Rare:61 | ||||
| chr5:178895886-178895927 | Rare:13 | ||||
| chr5:178940948-178941256 | Common:1; Rare:80 | ||||
| chr5:179023702-179023867 | Common:1; Rare:52 | ||||
| chr5:179559560-179559803 | Common:1; Rare:71 | ||||
| chr5:179623616-179623988 | Common:4; Rare:135 | ||||
| chr5:179698661-179699090 | Common:4; Rare:141 | ||||
| chr5:179806900-179807035 | Common:3; Rare:46 | ||||
| chr5:179858797-179859047 | Rare:133 | ||||
| chr5:180810102-180810229 | Common:1; Rare:28 | ||||
| chr5:180861210-180861394 | Common:2; Rare:77 | ||||
| chr5:181223132-181223309 | Rare:60 | ||||
| chr5:181223628-181223749 | Common:3; Rare:30 | ||||
| chr5:181261060-181261286 | Rare:78 |