| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177022635-177022732 | Rare:32 | ||||
| chr5:177133445-177133844 | Rare:143 | ||||
| chr5:177303678-177304039 | Common:3; Rare:141 | ||||
| chr5:177351643-177351968 | Rare:82 | ||||
| chr5:177367030-177367345 | Common:2; Rare:74 | ||||
| chr5:177497575-177497886 | Common:1; Rare:109 | ||||
| chr5:177600017-177600151 | Common:3; Rare:39 | ||||
| chr5:178153818-178154091 | Rare:84; Clinvar:4; Clinvar (benign):1 | ||||
| chr5:178204339-178204534 | Common:3; Rare:68 | ||||
| chr5:179060267-179060427 | Common:1; Rare:42 | ||||
| chr5:179550527-179550858 | Common:2; Rare:151 | ||||
| chr5:179559560-179559771 | Common:1; Rare:60 | ||||
| chr5:179698667-179699091 | Common:4; Rare:138 | ||||
| chr5:179806318-179806448 | Rare:41 | ||||
| chr5:179806905-179807063 | Common:3; Rare:53 |