| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:56815435-56815571 | Common:1; Rare:65 | ||||
| chr5:56909476-56909638 | Common:1; Rare:45 | ||||
| chr5:56909875-56910132 | Rare:75 | ||||
| chr5:56952076-56952265 | Rare:64 | ||||
| chr5:57173524-57174205 | Common:3; Rare:237 | ||||
| chr5:60700050-60700275 | Common:4; Rare:87 | ||||
| chr5:60844155-60844472 | Common:5; Rare:105 | ||||
| chr5:60944969-60945341 | Common:6; Rare:147; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr5:61162206-61162676 | Common:1; Rare:108 | ||||
| chr5:62305890-62306328 | Common:4; Rare:175 | ||||
| chr5:62306349-62306533 | Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:62403825-62404042 | Common:3; Rare:73 | ||||
| chr5:62412480-62412878 | Common:1; Rare:134 | ||||
| chr5:64689895-64690249 | Common:1; Rare:51 | ||||
| chr5:64768425-64769023 | Common:6; Rare:164 |