| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:58459985-58460245 | Common:6; Rare:106 | ||||
| chr5:59768269-59768435 | Common:1; Rare:44 | ||||
| chr5:59768517-59768762 | Rare:60 | ||||
| chr5:59768819-59768874 | Rare:9 | ||||
| chr5:60488061-60488359 | Rare:54 | ||||
| chr5:60945022-60945283 | Common:5; Rare:99; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr5:61162215-61162506 | Common:1; Rare:61 | ||||
| chr5:61162561-61162701 | Rare:28 | ||||
| chr5:62403507-62403561 | Rare:12 | ||||
| chr5:62403783-62404033 | Common:3; Rare:95 | ||||
| chr5:62412505-62412784 | Rare:90 | ||||
| chr5:64768423-64768457 | Common:1; Rare:10 | ||||
| chr5:64768507-64768977 | Common:5; Rare:132 | ||||
| chr5:65563091-65563449 | Common:4; Rare:136 | ||||
| chr5:65624620-65624808 | Common:9; Rare:30 |