| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176416322-176416653 | Common:1; Rare:100 | ||||
| chr5:176448109-176448410 | Common:1; Rare:107 | ||||
| chr5:176537844-176538127 | Common:1; Rare:90 | ||||
| chr5:177022642-177022741 | Rare:37 | ||||
| chr5:177133450-177133800 | Rare:123 | ||||
| chr5:177303654-177304059 | Common:4; Rare:156 | ||||
| chr5:177367048-177367331 | Common:2; Rare:65 | ||||
| chr5:177497545-177497870 | Common:1; Rare:118 | ||||
| chr5:177516889-177517019 | Common:2; Rare:63; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:178153771-178154170 | Rare:113; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204280-178204534 | Common:4; Rare:93 | ||||
| chr5:179559556-179559781 | Common:1; Rare:63 | ||||
| chr5:179698551-179699091 | Common:4; Rare:189 | ||||
| chr5:179820704-179820912 | Common:5; Rare:71; Clinvar (benign):1 | ||||
| chr5:179858798-179858945 | Rare:84 |