| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303667-177303966 | Common:4; Rare:126 | ||||
| chr5:177351609-177351737 | Rare:42 | ||||
| chr5:177371001-177371215 | Common:20; Rare:144 | ||||
| chr5:177404413-177404527 | Rare:39 | ||||
| chr5:177446485-177446853 | Common:2; Rare:101 | ||||
| chr5:177447897-177448084 | Common:2; Rare:38 | ||||
| chr5:177460432-177460705 | Common:1; Rare:90 | ||||
| chr5:177473438-177473747 | Common:1; Rare:106 | ||||
| chr5:177516877-177517084 | Common:2; Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177599851-177600216 | Common:4; Rare:104; Clinvar (benign):5 | ||||
| chr5:178153663-178153748 | Rare:30; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:178153776-178154111 | Rare:100; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204339-178204631 | Common:4; Rare:119 | ||||
| chr5:178232331-178232423 | Common:1; Rare:43 | ||||
| chr5:178232540-178232890 | Common:4; Rare:116 |