| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177303678-177304013 | Common:3; Rare:133 | ||||
| chr5:177351809-177352014 | Rare:48 | ||||
| chr5:177367222-177367325 | Common:1; Rare:16 | ||||
| chr5:177371046-177371185 | Common:18; Rare:114 | ||||
| chr5:177403937-177404219 | Common:3; Rare:104; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr5:177497591-177497861 | Common:1; Rare:98 | ||||
| chr5:177516889-177517093 | Common:2; Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177592000-177592295 | Common:2; Rare:117; Clinvar:1 | ||||
| chr5:178130917-178131039 | Rare:31 | ||||
| chr5:178153797-178154170 | Rare:102; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204337-178204546 | Common:3; Rare:73 | ||||
| chr5:179550501-179550563 | Common:2; Rare:24 | ||||
| chr5:179559560-179559814 | Common:1; Rare:74 | ||||
| chr5:179623595-179623988 | Common:4; Rare:140 | ||||
| chr5:179698561-179699109 | Common:4; Rare:192 |