| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179800247-179800598 | Common:2; Rare:107 | ||||
| chr5:179803316-179803418 | Common:1; Rare:19 | ||||
| chr5:179804753-179805024 | Common:1; Rare:63 | ||||
| chr5:179805051-179805458 | Common:2; Rare:88 | ||||
| chr5:179806292-179806450 | Rare:50 | ||||
| chr5:179806494-179806708 | Common:1; Rare:66 | ||||
| chr5:179806809-179807070 | Common:3; Rare:95 | ||||
| chr5:179821057-179821141 | Common:1; Rare:25; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:179823969-179824313 | Common:1; Rare:140; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr5:179858797-179858993 | Rare:108 | ||||
| chr5:180291911-180292196 | Common:2; Rare:103 | ||||
| chr5:180494205-180494524 | Common:4; Rare:109 | ||||
| chr5:180802713-180802953 | Common:7; Rare:97 | ||||
| chr5:180809823-180809946 | Common:4; Rare:26 | ||||
| chr5:180810108-180810229 | Common:1; Rare:27 |