| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:178153663-178154002 | Rare:117; Clinvar:8; Clinvar (benign):2 | ||||
| chr5:178204458-178204653 | Common:2; Rare:90 | ||||
| chr5:178232388-178232492 | Common:5; Rare:65 | ||||
| chr5:179550618-179550872 | Rare:115 | ||||
| chr5:179559556-179559819 | Common:1; Rare:77 | ||||
| chr5:179617540-179617922 | Rare:92 | ||||
| chr5:179617983-179618337 | Common:2; Rare:100 | ||||
| chr5:179621240-179621859 | Common:4; Rare:163 | ||||
| chr5:179622725-179622982 | Common:4; Rare:94 | ||||
| chr5:179698641-179699097 | Common:4; Rare:155 | ||||
| chr5:179806318-179806479 | Rare:57 | ||||
| chr5:179806830-179807099 | Common:3; Rare:95 | ||||
| chr5:179823857-179824318 | Common:1; Rare:191; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:180291928-180292251 | Common:2; Rare:133 | ||||
| chr5:180494199-180494429 | Common:2; Rare:67 |