| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177022600-177022736 | Common:1; Rare:54 | ||||
| chr5:177133453-177133853 | Rare:145 | ||||
| chr5:177303672-177304034 | Common:4; Rare:144 | ||||
| chr5:177367131-177367339 | Common:2; Rare:40 | ||||
| chr5:177496853-177497029 | Common:3; Rare:43 | ||||
| chr5:177516932-177517093 | Rare:56; Clinvar (pathogenic):1 | ||||
| chr5:177600021-177600159 | Common:3; Rare:43 | ||||
| chr5:178130891-178131039 | Rare:37 | ||||
| chr5:178153818-178154170 | Rare:98; Clinvar:4; Clinvar (benign):1 | ||||
| chr5:178232551-178232890 | Common:4; Rare:110 | ||||
| chr5:178626984-178627235 | Common:7; Rare:90 | ||||
| chr5:178859753-178860086 | Common:4; Rare:95 | ||||
| chr5:178941010-178941242 | Common:1; Rare:63 | ||||
| chr5:179023674-179023843 | Common:2; Rare:49 | ||||
| chr5:179060277-179060606 | Common:3; Rare:75 |