| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73058303-73058656 | Common:3; Rare:106 | ||||
| chr14:73136200-73136564 | Common:5; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73268390-73268704 | Common:1; Rare:84 | ||||
| chr14:73287258-73287366 | Rare:19 | ||||
| chr14:73457902-73458011 | Rare:30 | ||||
| chr14:73458513-73458857 | Common:5; Rare:90 | ||||
| chr14:73463551-73463773 | Common:1; Rare:39 | ||||
| chr14:73569008-73569294 | Rare:65 | ||||
| chr14:73592029-73592176 | Common:2; Rare:58 | ||||
| chr14:73760284-73760586 | Common:3; Rare:51 | ||||
| chr14:73787121-73787379 | Common:2; Rare:88 | ||||
| chr14:73851794-73851994 | Common:4; Rare:66 | ||||
| chr14:73950053-73950351 | Common:6; Rare:136; Clinvar (benign):4 | ||||
| chr14:74019201-74019450 | Common:2; Rare:96 | ||||
| chr14:74493240-74493795 | Common:4; Rare:181; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 |