| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:173328342-173328605 | Rare:54 | ||||
| chr5:176361615-176361890 | Rare:74 | ||||
| chr5:176388550-176388838 | Common:4; Rare:114 | ||||
| chr5:176448045-176448410 | Common:1; Rare:116 | ||||
| chr5:177022642-177022746 | Rare:38 | ||||
| chr5:177133459-177133800 | Rare:121 | ||||
| chr5:177303655-177303994 | Common:4; Rare:141 | ||||
| chr5:177497555-177497802 | Common:1; Rare:94 | ||||
| chr5:177516932-177517079 | Rare:51; Clinvar (pathogenic):1 | ||||
| chr5:178130823-178131047 | Rare:62 | ||||
| chr5:178204243-178204534 | Common:5; Rare:106 | ||||
| chr5:178626992-178627298 | Common:8; Rare:105 | ||||
| chr5:178940990-178941239 | Common:1; Rare:68 | ||||
| chr5:179559560-179559788 | Common:1; Rare:65 | ||||
| chr5:179623597-179624040 | Common:5; Rare:157 |