| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177006552-177006857 | Common:3; Rare:90 | ||||
| chr5:177022600-177022790 | Common:1; Rare:78 | ||||
| chr5:177044307-177044489 | Rare:39 | ||||
| chr5:177303615-177303811 | Common:4; Rare:80 | ||||
| chr5:177311841-177312105 | Common:1; Rare:91 | ||||
| chr5:177351590-177351688 | Rare:41 | ||||
| chr5:177460629-177460748 | Rare:42 | ||||
| chr5:177467480-177468220 | Common:3; Rare:241 | ||||
| chr5:177484482-177484522 | Rare:10 | ||||
| chr5:177484524-177484873 | Common:3; Rare:65 | ||||
| chr5:177492353-177492680 | Common:1; Rare:127 | ||||
| chr5:177496707-177497003 | Rare:62 | ||||
| chr5:177497329-177497355 | Rare:6 | ||||
| chr5:177497545-177497860 | Common:1; Rare:117 | ||||
| chr5:177516845-177517079 | Common:2; Rare:99; Clinvar:1; Clinvar (pathogenic):1 |