| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50312203-50312329 | Rare:43 | ||||
| chr14:50668287-50668556 | Common:3; Rare:97 | ||||
| chr14:50944378-50944573 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51651636-51651958 | Common:4; Rare:91 | ||||
| chr14:52003917-52004227 | Common:2; Rare:101 | ||||
| chr14:52069038-52069247 | Common:2; Rare:44 | ||||
| chr14:52314108-52314333 | Common:1; Rare:61 | ||||
| chr14:52695523-52695839 | Common:1; Rare:89 | ||||
| chr14:52707081-52707226 | Common:1; Rare:61 | ||||
| chr14:52791427-52791757 | Common:1; Rare:111 | ||||
| chr14:53152371-53152424 | Rare:20 | ||||
| chr14:53956814-53957012 | Rare:47 | ||||
| chr14:54488934-54489167 | Common:1; Rare:68 | ||||
| chr14:55027085-55027320 | Common:2; Rare:61 | ||||
| chr14:55129126-55129296 | Rare:50 |