| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:64987080-64987262 | Rare:71 | ||||
| chr14:65102285-65102575 | Common:2; Rare:95; Clinvar:5; Clinvar (benign):10 | ||||
| chr14:65411637-65411916 | Common:3; Rare:66 | ||||
| chr14:66507824-66508206 | Rare:157 | ||||
| chr14:66508379-66508549 | Rare:57 | ||||
| chr14:67241040-67241488 | Common:3; Rare:120 | ||||
| chr14:67359655-67360062 | Common:1; Rare:145 | ||||
| chr14:67360262-67360448 | Common:2; Rare:60 | ||||
| chr14:67382274-67382579 | Common:1; Rare:57 | ||||
| chr14:67412027-67412369 | Common:3; Rare:78 | ||||
| chr14:67533050-67533160 | Rare:25 | ||||
| chr14:67600185-67600333 | Common:5; Rare:57; Clinvar (pathogenic):1 | ||||
| chr14:67674375-67674656 | Common:2; Rare:90 | ||||
| chr14:67695630-67695803 | Rare:72 | ||||
| chr14:68000096-68000271 | Common:1; Rare:34; Clinvar (benign):1 |