| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:114314097-114315014 | Common:10; Rare:929 | ||||
| chr14:20305443-20305955 | Rare:224 | ||||
| chr14:20330879-20331476 | Common:4; Rare:124 | ||||
| chr14:20332300-20333051 | Common:2; Rare:241 | ||||
| chr14:20333160-20333560 | Common:3; Rare:152 | ||||
| chr14:20342920-20343742 | Common:97; Rare:2186 | ||||
| chr14:20412812-20413566 | Common:31; Rare:441 | ||||
| chr14:20413758-20414218 | Rare:131 | ||||
| chr14:20454233-20454711 | Rare:245 | ||||
| chr14:20454709-20455900 | Common:38; Rare:1172 | ||||
| chr14:20461187-20462061 | Common:36; Rare:1252 | ||||
| chr14:20469136-20469536 | Common:4; Rare:181; Clinvar:7; Clinvar (benign):3 | ||||
| chr14:20469580-20470341 | Common:4; Rare:198 | ||||
| chr14:20609408-20609568 | Common:3; Rare:58 | ||||
| chr14:20609975-20610375 | Common:7; Rare:245 |