| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75002662-75002982 | Common:1; Rare:105; Clinvar:2 | ||||
| chr14:75051409-75051510 | Common:1; Rare:30; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:75063958-75064184 | Common:1; Rare:57 | ||||
| chr14:75069477-75069710 | Common:1; Rare:56 | ||||
| chr14:75126902-75127132 | Rare:85 | ||||
| chr14:75176356-75176666 | Rare:95 | ||||
| chr14:75427653-75427731 | Rare:19 | ||||
| chr14:75660781-75661009 | Rare:62 | ||||
| chr14:75661145-75661601 | Common:5; Rare:121 | ||||
| chr14:75985705-75985807 | Rare:51; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr14:76151777-76151984 | Rare:72 | ||||
| chr14:76762496-76762634 | Rare:26 | ||||
| chr14:76762648-76762852 | Rare:63 | ||||
| chr14:76812525-76812615 | Common:1; Rare:19 | ||||
| chr14:76812782-76813018 | Common:1; Rare:96 |