| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73389308-73389334 | Common:1; Rare:2 | ||||
| chr14:73440463-73440502 | Common:2; Rare:7 | ||||
| chr14:73492542-73492724 | Common:1; Rare:57 | ||||
| chr14:73711809-73711866 | Rare:13 | ||||
| chr14:73711891-73712283 | Common:4; Rare:80 | ||||
| chr14:73759352-73759504 | Rare:53 | ||||
| chr14:73785621-73785781 | Rare:39 | ||||
| chr14:73918262-73918311 | Rare:8 | ||||
| chr14:73976360-73976590 | Common:1; Rare:52 | ||||
| chr14:74027417-74027473 | Rare:5 | ||||
| chr14:74128976-74129226 | Common:1; Rare:37 | ||||
| chr14:74503222-74503609 | Common:2; Rare:143; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:74551719-74551835 | Common:1; Rare:24 | ||||
| chr14:74554102-74554126 | Rare:1 | ||||
| chr14:74555302-74555667 | Common:4; Rare:90; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |