| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73246802-73246992 | Rare:78 | ||||
| chr10:73247190-73247418 | Rare:132 | ||||
| chr10:73671640-73671683 | Rare:6 | ||||
| chr10:73730436-73730791 | Common:1; Rare:75 | ||||
| chr10:73743313-73743606 | Common:1; Rare:57 | ||||
| chr10:73765890-73766186 | Rare:70 | ||||
| chr10:73766202-73766407 | Common:1; Rare:45 | ||||
| chr10:73769028-73769322 | Rare:95 | ||||
| chr10:73844117-73844259 | Common:1; Rare:25 | ||||
| chr10:73911942-73912421 | Common:2; Rare:120; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:73913278-73913769 | Common:1; Rare:148; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:73914756-73915402 | Common:1; Rare:158; Clinvar (benign):4 | ||||
| chr10:73917489-73917524 | Rare:5; Clinvar:1 | ||||
| chr10:73999016-73999287 | Rare:60 | ||||
| chr10:74070666-74071081 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):8 |