| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:44961903-44962255 | Common:3; Rare:102 | ||||
| chr14:45253078-45253291 | Rare:56 | ||||
| chr14:49586317-49586772 | Common:1; Rare:238; Clinvar (benign):1 | ||||
| chr14:49598719-49599029 | Common:2; Rare:113 | ||||
| chr14:49620561-49620830 | Common:2; Rare:110; Clinvar:3 | ||||
| chr14:49688205-49688251 | Rare:16 | ||||
| chr14:49892912-49893125 | Rare:85 | ||||
| chr14:50116545-50116695 | Rare:71 | ||||
| chr14:50312201-50312374 | Rare:66 | ||||
| chr14:50668295-50668560 | Common:4; Rare:98 | ||||
| chr14:50944361-50944572 | Common:4; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51240154-51240294 | Rare:64 | ||||
| chr14:51651661-51651990 | Common:4; Rare:94 | ||||
| chr14:51860575-51860769 | Rare:57 | ||||
| chr14:51989374-51989633 | Common:2; Rare:79 |