| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:59275513-59276117 | Common:4; Rare:87 | ||||
| chr5:59276192-59276302 | Rare:26 | ||||
| chr5:59356812-59357084 | Common:1; Rare:63 | ||||
| chr5:59357089-59357163 | Common:1; Rare:10 | ||||
| chr5:59357213-59357545 | Common:3; Rare:64 | ||||
| chr5:59768505-59768910 | Rare:93 | ||||
| chr5:60448626-60448873 | Common:1; Rare:42 | ||||
| chr5:60487615-60487930 | Common:3; Rare:48 | ||||
| chr5:60487938-60488398 | Common:1; Rare:76 | ||||
| chr5:60700067-60700258 | Common:2; Rare:74 | ||||
| chr5:60945011-60945382 | Common:6; Rare:148; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr5:61162215-61162673 | Common:1; Rare:108 | ||||
| chr5:62403695-62404039 | Common:3; Rare:137 | ||||
| chr5:62412542-62412857 | Common:1; Rare:109 | ||||
| chr5:64768513-64769031 | Common:5; Rare:138 |