| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50944372-50944603 | Common:4; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51240124-51240325 | Rare:93 | ||||
| chr14:51651620-51651984 | Common:4; Rare:102 | ||||
| chr14:52069000-52069226 | Common:2; Rare:50 | ||||
| chr14:52314067-52314369 | Common:2; Rare:80 | ||||
| chr14:52695504-52695809 | Common:1; Rare:83 | ||||
| chr14:52707099-52707232 | Common:1; Rare:57 | ||||
| chr14:52791570-52791905 | Common:3; Rare:112 | ||||
| chr14:52951003-52951442 | Common:4; Rare:157 | ||||
| chr14:53152359-53152424 | Rare:26 | ||||
| chr14:53956736-53956986 | Rare:58; Clinvar:1 | ||||
| chr14:54488825-54489171 | Common:3; Rare:98 | ||||
| chr14:55027059-55027290 | Common:2; Rare:64 | ||||
| chr14:55051462-55051723 | Rare:111 | ||||
| chr14:55129119-55129298 | Common:1; Rare:50 |