| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:47626523-47626635 | Rare:48 | ||||
| chr14:49586317-49586766 | Common:1; Rare:235; Clinvar (benign):1 | ||||
| chr14:49586794-49586808 | Rare:3 | ||||
| chr14:49598639-49599000 | Common:3; Rare:142 | ||||
| chr14:49620470-49620854 | Common:3; Rare:136; Clinvar:4 | ||||
| chr14:49621051-49621419 | Rare:117; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:49688169-49688326 | Rare:62 | ||||
| chr14:49693002-49693188 | Common:1; Rare:71 | ||||
| chr14:49767583-49767688 | Common:1; Rare:36 | ||||
| chr14:49768715-49768845 | Rare:36 | ||||
| chr14:49800633-49800923 | Common:1; Rare:68 | ||||
| chr14:49892875-49893142 | Rare:119 | ||||
| chr14:50116524-50116696 | Rare:92 | ||||
| chr14:50231879-50232010 | Common:1; Rare:53 | ||||
| chr14:50312100-50312387 | Common:1; Rare:124; Clinvar:1; Clinvar (benign):1 |