| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43556332-43556414 | Common:2; Rare:25 | ||||
| chr5:43602678-43602756 | Common:1; Rare:14 | ||||
| chr5:43603073-43603245 | Rare:43 | ||||
| chr5:44808727-44808971 | Common:2; Rare:82 | ||||
| chr5:50667767-50668027 | Common:1; Rare:76 | ||||
| chr5:53109711-53109897 | Common:1; Rare:95; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:53560611-53560755 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:55233603-55233899 | Common:5; Rare:108 | ||||
| chr5:55307394-55308153 | Common:5; Rare:287 | ||||
| chr5:55994794-55995198 | Rare:137 | ||||
| chr5:56952092-56952227 | Rare:40 | ||||
| chr5:57173553-57173951 | Common:2; Rare:144 | ||||
| chr5:57173994-57174319 | Common:1; Rare:89 | ||||
| chr5:58455461-58455551 | Rare:19 | ||||
| chr5:59039011-59039136 | Common:1; Rare:38; Clinvar (benign):1 |