| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50668327-50668556 | Common:3; Rare:85 | ||||
| chr14:50944399-50944604 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51651734-51651984 | Common:4; Rare:72 | ||||
| chr14:52068980-52069224 | Common:2; Rare:59 | ||||
| chr14:52314108-52314319 | Common:1; Rare:57 | ||||
| chr14:52695510-52695779 | Common:1; Rare:68 | ||||
| chr14:52707082-52707239 | Common:1; Rare:69 | ||||
| chr14:52791418-52791889 | Common:3; Rare:148 | ||||
| chr14:53152380-53152424 | Rare:16 | ||||
| chr14:55027057-55027290 | Common:2; Rare:64 | ||||
| chr14:55051462-55051748 | Rare:125 | ||||
| chr14:55191538-55191750 | Common:5; Rare:47 | ||||
| chr14:55411762-55411963 | Common:2; Rare:105 | ||||
| chr14:55580093-55580285 | Common:2; Rare:84 | ||||
| chr14:57268526-57268604 | Rare:20 |