| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:54440989-54441012 | Rare:8 | ||||
| chr14:54441311-54441771 | Common:1; Rare:135 | ||||
| chr14:54488797-54489308 | Common:4; Rare:126 | ||||
| chr14:54509554-54509978 | Common:6; Rare:142 | ||||
| chr14:54566936-54567180 | Rare:64 | ||||
| chr14:54567505-54567794 | Common:2; Rare:59 | ||||
| chr14:54902128-54902399 | Common:2; Rare:92; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr14:54902802-54902992 | Rare:58; Clinvar (benign):1 | ||||
| chr14:55026975-55027366 | Common:2; Rare:104 | ||||
| chr14:55051352-55051779 | Common:2; Rare:172 | ||||
| chr14:55051930-55052193 | Common:1; Rare:83 | ||||
| chr14:55129053-55129277 | Common:1; Rare:56 | ||||
| chr14:55129575-55129938 | Common:1; Rare:79 | ||||
| chr14:55191313-55191397 | Rare:16 | ||||
| chr14:55191479-55191862 | Common:7; Rare:99 |