| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:65413150-65413212 | Rare:4 | ||||
| chr14:66507811-66508180 | Rare:143 | ||||
| chr14:66508323-66508530 | Rare:65 | ||||
| chr14:67241117-67241491 | Common:1; Rare:96 | ||||
| chr14:67359694-67360052 | Common:1; Rare:126 | ||||
| chr14:67360245-67360368 | Common:1; Rare:35 | ||||
| chr14:67382184-67382453 | Common:1; Rare:46 | ||||
| chr14:67412109-67412335 | Common:1; Rare:51 | ||||
| chr14:67585671-67585993 | Common:1; Rare:72 | ||||
| chr14:67600199-67600468 | Common:6; Rare:93; Clinvar (pathogenic):1 | ||||
| chr14:67619646-67619968 | Common:2; Rare:83 | ||||
| chr14:67674400-67674417 | Rare:6 | ||||
| chr14:67674430-67674933 | Common:2; Rare:136 | ||||
| chr14:67816546-67816732 | Rare:34; Clinvar:1 | ||||
| chr14:68792874-68793381 | Common:2; Rare:152 |