| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176388569-176388885 | Common:5; Rare:122 | ||||
| chr5:176448106-176448410 | Common:1; Rare:108 | ||||
| chr5:176529360-176529554 | Common:1; Rare:74 | ||||
| chr5:176537861-176538129 | Common:1; Rare:87 | ||||
| chr5:176543506-176543667 | Rare:46 | ||||
| chr5:176549208-176549405 | Rare:50 | ||||
| chr5:177022610-177022810 | Rare:78 | ||||
| chr5:177133495-177133872 | Rare:136 | ||||
| chr5:177303678-177303881 | Common:3; Rare:95 | ||||
| chr5:177351847-177352014 | Rare:38 | ||||
| chr5:177371031-177371099 | Common:14; Rare:63 | ||||
| chr5:177403179-177403214 | Rare:7 | ||||
| chr5:177496836-177497095 | Common:3; Rare:58 | ||||
| chr5:177516908-177517084 | Common:1; Rare:65; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:178130872-178131040 | Rare:44 |