| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:58459492-58460090 | Common:4; Rare:203 | ||||
| chr5:59768487-59768719 | Rare:61 | ||||
| chr5:59768726-59769053 | Rare:53 | ||||
| chr5:60700091-60700240 | Common:1; Rare:57 | ||||
| chr5:60944933-60945410 | Common:6; Rare:191; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr5:61162217-61162659 | Common:1; Rare:104 | ||||
| chr5:62361246-62361492 | Common:1; Rare:40; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr5:62403821-62404044 | Common:3; Rare:78 | ||||
| chr5:62412545-62412878 | Common:1; Rare:112 | ||||
| chr5:64768524-64769078 | Common:5; Rare:140 | ||||
| chr5:65481384-65481489 | Common:1; Rare:30 | ||||
| chr5:65481511-65481649 | Rare:34 | ||||
| chr5:65481706-65482036 | Common:1; Rare:61 | ||||
| chr5:65563091-65563463 | Common:4; Rare:142 | ||||
| chr5:65624634-65624816 | Common:8; Rare:27 |