| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49868129-49868453 | Common:3; Rare:72 | ||||
| chr14:52315347-52315642 | Rare:64 | ||||
| chr14:54565833-54565966 | Rare:32 | ||||
| chr14:54730583-54730795 | Common:1; Rare:25 | ||||
| chr14:58266597-58266920 | Common:2; Rare:56 | ||||
| chr14:61472145-61472469 | Common:1; Rare:58 | ||||
| chr14:61480159-61480425 | Common:1; Rare:43 | ||||
| chr14:61562892-61563165 | Common:1; Rare:44 | ||||
| chr14:61564632-61564796 | Common:1; Rare:38 | ||||
| chr14:61565945-61566126 | Rare:28 | ||||
| chr14:61721572-61721802 | Common:1; Rare:41 | ||||
| chr14:61751065-61751232 | Rare:45 | ||||
| chr14:63854082-63854104 | Rare:4 | ||||
| chr14:63941703-63941928 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:64165213-64165345 | Rare:37; Clinvar:3; Clinvar (benign):1 |