| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:64431277-64431629 | Common:2; Rare:77 | ||||
| chr14:64503609-64503887 | Common:2; Rare:107 | ||||
| chr14:64504149-64504337 | Common:2; Rare:59 | ||||
| chr14:64504574-64504860 | Rare:85 | ||||
| chr14:64505228-64505483 | Common:1; Rare:59 | ||||
| chr14:64540484-64540753 | Common:2; Rare:71 | ||||
| chr14:64914229-64914533 | Common:3; Rare:114 | ||||
| chr14:64942503-64942844 | Rare:105 | ||||
| chr14:64942846-64942873 | Rare:6 | ||||
| chr14:64972124-64972403 | Common:5; Rare:75 | ||||
| chr14:64986838-64986935 | Rare:39 | ||||
| chr14:64987093-64987284 | Rare:69 | ||||
| chr14:65102137-65102833 | Common:10; Rare:204; Clinvar:5; Clinvar (benign):10 | ||||
| chr14:65411811-65411981 | Common:2; Rare:55 | ||||
| chr14:65412532-65413148 | Common:6; Rare:175 |