| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:63852894-63853033 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:64196953-64197034 | Rare:23 | ||||
| chr14:64387938-64388413 | Common:2; Rare:165 | ||||
| chr14:64503592-64503887 | Common:2; Rare:112 | ||||
| chr14:64504553-64504842 | Rare:86 | ||||
| chr14:64505230-64505369 | Rare:34 | ||||
| chr14:64914234-64914533 | Common:3; Rare:113 | ||||
| chr14:64987082-64987284 | Rare:76 | ||||
| chr14:65102360-65102866 | Common:9; Rare:141; Clinvar:3; Clinvar (benign):5 | ||||
| chr14:65411754-65411921 | Common:2; Rare:44 | ||||
| chr14:65412512-65412913 | Common:6; Rare:130 | ||||
| chr14:66507809-66508215 | Rare:167 | ||||
| chr14:66508419-66508530 | Rare:46 | ||||
| chr14:67241080-67241540 | Common:2; Rare:124 | ||||
| chr14:67359738-67360079 | Common:1; Rare:109 |