| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:59039275-59039662 | Common:3; Rare:88 | ||||
| chr5:59039773-59040015 | Common:2; Rare:68 | ||||
| chr5:59275455-59275877 | Common:1; Rare:65 | ||||
| chr5:59275889-59276001 | Common:2; Rare:13 | ||||
| chr5:59586672-59586796 | Rare:20 | ||||
| chr5:59768289-59768893 | Common:1; Rare:155 | ||||
| chr5:59768990-59769051 | Rare:8 | ||||
| chr5:60487995-60487999 | |||||
| chr5:60488061-60488207 | Rare:24 | ||||
| chr5:60700058-60700218 | Rare:65 | ||||
| chr5:60844169-60844472 | Common:5; Rare:101 | ||||
| chr5:60944935-60945404 | Common:6; Rare:188; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr5:61162215-61162628 | Common:1; Rare:100 | ||||
| chr5:61331865-61332182 | Rare:122 | ||||
| chr5:61332602-61332930 | Common:3; Rare:109; Clinvar:2 |