| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177351633-177351958 | Rare:87 | ||||
| chr5:177496853-177497074 | Common:3; Rare:49 | ||||
| chr5:177497545-177497865 | Common:1; Rare:118 | ||||
| chr5:177516932-177517084 | Rare:52; Clinvar (pathogenic):1 | ||||
| chr5:177599979-177600224 | Common:4; Rare:80; Clinvar (benign):5 | ||||
| chr5:178204362-178204534 | Common:3; Rare:59 | ||||
| chr5:178232551-178232908 | Common:4; Rare:119 | ||||
| chr5:178627014-178627235 | Common:7; Rare:78 | ||||
| chr5:179060304-179060388 | Common:1; Rare:17 | ||||
| chr5:179559559-179559814 | Common:1; Rare:74 | ||||
| chr5:179698610-179699095 | Common:4; Rare:171 | ||||
| chr5:179806864-179807063 | Common:3; Rare:79 | ||||
| chr5:179820713-179820907 | Common:5; Rare:66; Clinvar (benign):1 | ||||
| chr5:179858797-179859031 | Rare:123 | ||||
| chr5:179907828-179908006 | Common:2; Rare:92 |