| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49620962-49621314 | Common:1; Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:49634687-49634950 | Rare:108; Clinvar:10; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49635179-49635337 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr14:49687992-49688364 | Common:2; Rare:132 | ||||
| chr14:49692966-49693281 | Common:1; Rare:124 | ||||
| chr14:49693342-49693613 | Common:1; Rare:91 | ||||
| chr14:49767434-49767452 | Rare:3 | ||||
| chr14:49767484-49767775 | Common:2; Rare:98 | ||||
| chr14:49767878-49768279 | Common:3; Rare:138 | ||||
| chr14:49768488-49768636 | Rare:57 | ||||
| chr14:49768661-49768990 | Rare:87 | ||||
| chr14:49852390-49852478 | Rare:27 | ||||
| chr14:49852759-49852996 | Common:3; Rare:66 | ||||
| chr14:49853000-49853149 | Rare:30 | ||||
| chr14:49892389-49892642 | Common:1; Rare:63 |