| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50396994-50397120 | Common:1; Rare:58 | ||||
| chr14:50397247-50397325 | Rare:22 | ||||
| chr14:50532064-50532182 | Rare:25 | ||||
| chr14:50532450-50532810 | Common:4; Rare:109 | ||||
| chr14:50533105-50533300 | Common:1; Rare:31 | ||||
| chr14:50667774-50667941 | Rare:71 | ||||
| chr14:50668086-50668138 | Rare:17 | ||||
| chr14:50668160-50668801 | Common:17; Rare:278 | ||||
| chr14:50831105-50831296 | Common:1; Rare:65 | ||||
| chr14:50944102-50944288 | Common:1; Rare:67; Clinvar (benign):2 | ||||
| chr14:50944363-50944675 | Common:6; Rare:106; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51095038-51095553 | Common:5; Rare:179 | ||||
| chr14:51240001-51240375 | Common:2; Rare:135 | ||||
| chr14:51240427-51240545 | Common:2; Rare:46 | ||||
| chr14:51240586-51240676 | Common:1; Rare:32 |