| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50116557-50116641 | Rare:45 | ||||
| chr14:50312201-50312374 | Rare:66 | ||||
| chr14:50532503-50532698 | Common:2; Rare:57 | ||||
| chr14:50668295-50668556 | Common:3; Rare:95 | ||||
| chr14:50944399-50944638 | Common:4; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51240126-51240295 | Rare:75 | ||||
| chr14:51651611-51651964 | Common:4; Rare:95 | ||||
| chr14:51989376-51989676 | Common:2; Rare:96 | ||||
| chr14:52069000-52069232 | Common:2; Rare:51 | ||||
| chr14:52314101-52314376 | Common:1; Rare:74 | ||||
| chr14:52695512-52695812 | Common:1; Rare:81 | ||||
| chr14:52707057-52707229 | Common:1; Rare:75 | ||||
| chr14:52791427-52791778 | Common:2; Rare:116 | ||||
| chr14:52951009-52951442 | Common:4; Rare:154 | ||||
| chr14:55027059-55027290 | Common:2; Rare:64 |