| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1584250-1584301 | Common:4; Rare:6 | ||||
| chr5:1594426-1594762 | Common:5; Rare:123 | ||||
| chr5:1633927-1634076 | Common:2; Rare:57 | ||||
| chr5:2756386-2756588 | Rare:57 | ||||
| chr5:7883071-7883268 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:8457562-8457741 | Common:2; Rare:60 | ||||
| chr5:13923316-13923560 | Common:1; Rare:65; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr5:14011727-14011888 | Common:2; Rare:54 | ||||
| chr5:15902117-15902273 | Rare:27 | ||||
| chr5:32048412-32048585 | Common:1; Rare:43 | ||||
| chr5:32071948-32072279 | Common:2; Rare:84 | ||||
| chr5:32102234-32102437 | Common:2; Rare:38 | ||||
| chr5:32173247-32173422 | Common:2; Rare:42 | ||||
| chr5:34244691-34244925 | Rare:62 | ||||
| chr5:37063677-37063820 | Common:2; Rare:29 |