| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:87992988-87993324 | Common:5; Rare:156; Clinvar:14; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr14:88562917-88563126 | Rare:98 | ||||
| chr14:88824343-88824716 | Common:2; Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:88824777-88824883 | Rare:35 | ||||
| chr14:89350150-89350326 | Rare:35 | ||||
| chr14:89954640-89954950 | Rare:96 | ||||
| chr14:90331900-90332235 | Common:1; Rare:99 | ||||
| chr14:90397002-90397232 | Common:5; Rare:112; Clinvar (benign):2 | ||||
| chr14:91060122-91060310 | Common:2; Rare:51 | ||||
| chr14:91113982-91114131 | Rare:44 | ||||
| chr14:91114257-91114402 | Rare:29 | ||||
| chr14:91244672-91244829 | Common:2; Rare:28 | ||||
| chr14:91510226-91510652 | Common:1; Rare:140 | ||||
| chr14:92040011-92040159 | Common:3; Rare:45; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:92121649-92122014 | Common:5; Rare:126 |