| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177367131-177367379 | Common:2; Rare:57 | ||||
| chr5:177371039-177371105 | Common:17; Rare:73 | ||||
| chr5:177497552-177497865 | Common:1; Rare:116 | ||||
| chr5:177516870-177517093 | Common:2; Rare:90; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177592376-177592645 | Common:1; Rare:83 | ||||
| chr5:178006783-178006893 | Common:1; Rare:13 | ||||
| chr5:178153813-178154116 | Rare:92; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204362-178204534 | Common:3; Rare:59 | ||||
| chr5:178232546-178232873 | Common:4; Rare:109 | ||||
| chr5:178590353-178590513 | Rare:41 | ||||
| chr5:178626535-178626643 | Common:2; Rare:27 | ||||
| chr5:178626944-178627228 | Common:5; Rare:88 | ||||
| chr5:178859749-178860123 | Common:4; Rare:105 | ||||
| chr5:178895775-178895946 | Common:1; Rare:57 | ||||
| chr5:178940948-178941267 | Common:1; Rare:85 |