| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177516895-177517068 | Common:2; Rare:71; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177600029-177600210 | Common:4; Rare:62; Clinvar (benign):5 | ||||
| chr5:178113386-178113668 | Common:3; Rare:89 | ||||
| chr5:178130882-178131033 | Rare:42 | ||||
| chr5:178204339-178204534 | Common:3; Rare:68 | ||||
| chr5:178627003-178627276 | Common:7; Rare:98 | ||||
| chr5:179060304-179060420 | Common:1; Rare:26 | ||||
| chr5:179559559-179559781 | Common:1; Rare:62 | ||||
| chr5:179698610-179699095 | Common:4; Rare:171 | ||||
| chr5:179806895-179807063 | Common:3; Rare:59 | ||||
| chr5:179820795-179820907 | Common:2; Rare:41; Clinvar (benign):1 | ||||
| chr5:179858797-179858969 | Rare:96 | ||||
| chr5:179907820-179908015 | Common:2; Rare:99 | ||||
| chr5:180802766-180802976 | Common:8; Rare:83 | ||||
| chr5:180810133-180810212 | Rare:15 |