| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177400610-177400721 | Common:2; Rare:33 | ||||
| chr5:177426209-177426563 | Common:3; Rare:106 | ||||
| chr5:177447780-177447961 | Common:2; Rare:40 | ||||
| chr5:177497545-177497785 | Common:1; Rare:90 | ||||
| chr5:177516863-177517100 | Common:2; Rare:94; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177554610-177554729 | Common:1; Rare:36 | ||||
| chr5:177592051-177592287 | Common:2; Rare:101 | ||||
| chr5:177599841-177600234 | Common:4; Rare:115; Clinvar (benign):5 | ||||
| chr5:177753242-177753459 | Rare:32 | ||||
| chr5:178006583-178006967 | Common:3; Rare:27 | ||||
| chr5:178130848-178131045 | Rare:54 | ||||
| chr5:178153675-178154110 | Rare:139; Clinvar:7; Clinvar (benign):2 | ||||
| chr5:178204337-178204534 | Common:3; Rare:69 | ||||
| chr5:178231244-178231363 | Rare:34 | ||||
| chr5:178232232-178232482 | Common:6; Rare:124 |