| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303678-177303922 | Common:3; Rare:107 | ||||
| chr5:177311857-177312048 | Common:1; Rare:60 | ||||
| chr5:177312265-177312462 | Rare:61 | ||||
| chr5:177351633-177351772 | Rare:40 | ||||
| chr5:177497555-177497865 | Common:1; Rare:115 | ||||
| chr5:177516889-177517066 | Common:2; Rare:73; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177599987-177600224 | Common:4; Rare:78; Clinvar (benign):5 | ||||
| chr5:178113348-178113676 | Common:5; Rare:105 | ||||
| chr5:178130823-178131026 | Rare:58 | ||||
| chr5:178153774-178154170 | Rare:111; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204337-178204537 | Common:3; Rare:69 | ||||
| chr5:178627014-178627237 | Common:7; Rare:78 | ||||
| chr5:178859753-178860007 | Common:1; Rare:75 | ||||
| chr5:179060212-179060495 | Common:2; Rare:72 | ||||
| chr5:179559560-179559788 | Common:1; Rare:65 |