| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:57173540-57174202 | Common:3; Rare:223 | ||||
| chr5:58459907-58460246 | Common:6; Rare:132 | ||||
| chr5:59039075-59039222 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr5:59275552-59275788 | Rare:34 | ||||
| chr5:59275984-59276181 | Common:4; Rare:28 | ||||
| chr5:59768267-59768354 | Rare:24 | ||||
| chr5:59768487-59768892 | Rare:97 | ||||
| chr5:60488014-60488165 | Common:1; Rare:22 | ||||
| chr5:60700084-60700237 | Common:1; Rare:59 | ||||
| chr5:60844175-60844448 | Common:5; Rare:90 | ||||
| chr5:60945017-60945380 | Common:6; Rare:145; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr5:61162215-61162518 | Common:1; Rare:67 | ||||
| chr5:61162532-61162673 | Rare:35 | ||||
| chr5:62403503-62403603 | Rare:27 | ||||
| chr5:62403731-62404042 | Common:3; Rare:120 |