| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176388569-176388822 | Common:4; Rare:103 | ||||
| chr5:176448188-176448405 | Common:1; Rare:78 | ||||
| chr5:177006680-177006941 | Common:2; Rare:87 | ||||
| chr5:177022594-177022741 | Common:1; Rare:60 | ||||
| chr5:177133448-177133800 | Rare:123 | ||||
| chr5:177303691-177303965 | Common:3; Rare:117 | ||||
| chr5:177351520-177351772 | Rare:86 | ||||
| chr5:177367190-177367331 | Common:1; Rare:24 | ||||
| chr5:177516932-177517089 | Rare:54; Clinvar (pathogenic):1 | ||||
| chr5:178153795-178154170 | Rare:103; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178626992-178627238 | Common:7; Rare:89 | ||||
| chr5:178940978-178941242 | Common:1; Rare:71 | ||||
| chr5:179060271-179060456 | Common:2; Rare:47 | ||||
| chr5:179559551-179559814 | Common:1; Rare:75 | ||||
| chr5:179623596-179623846 | Common:2; Rare:101 |