| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49688188-49688409 | Common:2; Rare:74 | ||||
| chr14:49768002-49768261 | Common:2; Rare:97 | ||||
| chr14:49892909-49893118 | Rare:82 | ||||
| chr14:50116551-50116699 | Rare:68 | ||||
| chr14:50312155-50312374 | Rare:93 | ||||
| chr14:50532495-50532782 | Common:3; Rare:96 | ||||
| chr14:50944321-50944572 | Common:4; Rare:96; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51095130-51095298 | Common:3; Rare:64 | ||||
| chr14:51240007-51240355 | Common:2; Rare:124 | ||||
| chr14:51651611-51651968 | Common:4; Rare:95 | ||||
| chr14:51989376-51989670 | Common:2; Rare:94 | ||||
| chr14:52707033-52707303 | Common:1; Rare:108 | ||||
| chr14:55027035-55027617 | Common:4; Rare:127 | ||||
| chr14:55051460-55051749 | Rare:126 | ||||
| chr14:55191513-55191768 | Common:5; Rare:62 |