| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43483837-43483959 | Common:1; Rare:43 | ||||
| chr5:43515133-43515203 | Common:2; Rare:19 | ||||
| chr5:43602549-43602741 | Common:2; Rare:35 | ||||
| chr5:43602886-43603285 | Rare:97 | ||||
| chr5:44808718-44808965 | Common:2; Rare:81 | ||||
| chr5:50441214-50441431 | Common:3; Rare:61 | ||||
| chr5:50667768-50667915 | Common:1; Rare:46 | ||||
| chr5:52787860-52787971 | Rare:20 | ||||
| chr5:52788024-52788242 | Common:1; Rare:44 | ||||
| chr5:52989216-52989383 | Common:4; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53109705-53109909 | Common:1; Rare:102; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310430-54310711 | Common:1; Rare:83 | ||||
| chr5:55233603-55233882 | Common:4; Rare:100 | ||||
| chr5:55307631-55308049 | Common:5; Rare:150 | ||||
| chr5:55534642-55534817 | Common:3; Rare:60 |