| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:175968279-175968606 | Common:1; Rare:36 | ||||
| chr5:176361748-176361969 | Common:3; Rare:60 | ||||
| chr5:176388529-176388809 | Common:4; Rare:112 | ||||
| chr5:176448162-176448405 | Common:1; Rare:86 | ||||
| chr5:177022635-177022741 | Rare:39 | ||||
| chr5:177133448-177133869 | Rare:149 | ||||
| chr5:177303672-177303888 | Common:4; Rare:101 | ||||
| chr5:177462275-177462560 | Common:1; Rare:63 | ||||
| chr5:177516886-177517065 | Common:2; Rare:74; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177600033-177600210 | Common:4; Rare:62; Clinvar (benign):5 | ||||
| chr5:178130868-178131026 | Rare:42 | ||||
| chr5:178153828-178154110 | Rare:82; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:178204337-178204534 | Common:3; Rare:69 | ||||
| chr5:178232566-178232886 | Common:4; Rare:103 | ||||
| chr5:178859883-178859974 | Rare:24 |