| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177133453-177133853 | Rare:145 | ||||
| chr5:177303678-177304075 | Common:3; Rare:148 | ||||
| chr5:177351483-177351688 | Rare:77 | ||||
| chr5:177351809-177352059 | Rare:65 | ||||
| chr5:177367183-177367379 | Common:2; Rare:44 | ||||
| chr5:177370848-177371221 | Common:21; Rare:215 | ||||
| chr5:177403252-177403618 | Common:2; Rare:117; Clinvar (benign):3 | ||||
| chr5:177405053-177405383 | Common:3; Rare:71; Clinvar (benign):3 | ||||
| chr5:177409469-177409635 | Common:2; Rare:50; Clinvar (benign):5 | ||||
| chr5:177497584-177497868 | Common:1; Rare:100 | ||||
| chr5:177516932-177517076 | Rare:50; Clinvar (pathogenic):1 | ||||
| chr5:177592376-177592620 | Common:1; Rare:78 | ||||
| chr5:177600014-177600242 | Common:4; Rare:74; Clinvar (benign):5 | ||||
| chr5:178204337-178204534 | Common:3; Rare:69 | ||||
| chr5:178232513-178232944 | Common:5; Rare:140 |