| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:70907940-70908254 | Common:1; Rare:96 | ||||
| chr14:71320140-71320637 | Rare:152 | ||||
| chr14:71321306-71321488 | Common:2; Rare:54 | ||||
| chr14:71321773-71321909 | Common:1; Rare:25 | ||||
| chr14:71598072-71598185 | Rare:25 | ||||
| chr14:72894083-72894276 | Common:4; Rare:65 | ||||
| chr14:72927045-72927230 | Common:1; Rare:42 | ||||
| chr14:73027032-73027407 | Common:2; Rare:94 | ||||
| chr14:73058204-73058635 | Common:3; Rare:136 | ||||
| chr14:73058704-73058934 | Common:1; Rare:55 | ||||
| chr14:73136370-73136572 | Common:4; Rare:71; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73136687-73137111 | Common:2; Rare:91 | ||||
| chr14:73457982-73458181 | Common:6; Rare:44 | ||||
| chr14:73458492-73458935 | Common:6; Rare:126 | ||||
| chr14:73463580-73463630 | Common:1; Rare:12 |