| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:51651550-51652120 | Common:9; Rare:263 | ||||
| chr14:51989374-51989671 | Common:4; Rare:188 | ||||
| chr14:52069033-52069299 | Common:2; Rare:93 | ||||
| chr14:52069570-52070250 | Common:8; Rare:163 | ||||
| chr14:52552398-52552844 | Common:2; Rare:243 | ||||
| chr14:52695485-52695851 | Common:2; Rare:191 | ||||
| chr14:52707040-52707242 | Common:2; Rare:168 | ||||
| chr14:52729826-52730257 | Common:2; Rare:131 | ||||
| chr14:52791404-52791884 | Common:4; Rare:266 | ||||
| chr14:52950980-52951442 | Common:8; Rare:310 | ||||
| chr14:53152210-53152610 | Rare:252; Clinvar (benign):5 | ||||
| chr14:53153155-53153413 | Common:6; Rare:176 | ||||
| chr14:54396728-54397076 | Common:4; Rare:189 | ||||
| chr14:54441307-54441513 | Rare:145 | ||||
| chr14:54441424-54441538 | Rare:34 |