| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:157731336-157731443 | Common:4; Rare:38 | ||||
| chr5:159207903-159207982 | Rare:20 | ||||
| chr5:159263189-159263321 | Common:1; Rare:40 | ||||
| chr5:160419042-160419253 | Common:4; Rare:81 | ||||
| chr5:160421709-160421900 | Common:1; Rare:49 | ||||
| chr5:163460327-163460660 | Common:5; Rare:75 | ||||
| chr5:172006617-172006950 | Common:1; Rare:72 | ||||
| chr5:176388519-176388742 | Common:1; Rare:80 | ||||
| chr5:176448195-176448405 | Common:1; Rare:76 | ||||
| chr5:177022626-177022771 | Rare:57 | ||||
| chr5:177303655-177303891 | Common:4; Rare:110 | ||||
| chr5:177351629-177351693 | Rare:20 | ||||
| chr5:177497575-177497859 | Common:1; Rare:104 | ||||
| chr5:177516863-177517073 | Common:2; Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:178153662-178153684 | Rare:11; Clinvar:1 |