| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:57173555-57173865 | Common:2; Rare:110 | ||||
| chr5:58460052-58460196 | Common:4; Rare:59 | ||||
| chr5:60488063-60488207 | Rare:23 | ||||
| chr5:60700102-60700240 | Common:1; Rare:53 | ||||
| chr5:60945026-60945258 | Common:5; Rare:87; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr5:61162404-61162555 | Common:1; Rare:46 | ||||
| chr5:62306143-62306469 | Common:3; Rare:126; Clinvar (benign):2 | ||||
| chr5:62403821-62404031 | Common:3; Rare:73 | ||||
| chr5:64768553-64768972 | Common:5; Rare:111 | ||||
| chr5:65563116-65563313 | Common:3; Rare:70 | ||||
| chr5:65624983-65625083 | Rare:39 | ||||
| chr5:65722066-65722360 | Common:4; Rare:99 | ||||
| chr5:69166927-69167192 | Common:2; Rare:62 | ||||
| chr5:69189509-69189611 | Common:1; Rare:33 | ||||
| chr5:69332783-69332865 | Rare:24 |