| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67412073-67412283 | Common:1; Rare:58 | ||||
| chr14:67532961-67533333 | Common:1; Rare:83 | ||||
| chr14:67599806-67600027 | Common:4; Rare:52 | ||||
| chr14:67600072-67600407 | Common:7; Rare:114; Clinvar (pathogenic):1 | ||||
| chr14:67619543-67619996 | Common:2; Rare:125 | ||||
| chr14:67674200-67674495 | Common:3; Rare:96 | ||||
| chr14:67674555-67674743 | Rare:49 | ||||
| chr14:67674778-67675138 | Common:3; Rare:83 | ||||
| chr14:67695496-67695848 | Common:1; Rare:123 | ||||
| chr14:67815949-67816196 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:67816339-67816363 | Rare:5 | ||||
| chr14:67816505-67816872 | Common:1; Rare:79; Clinvar:1 | ||||
| chr14:67819677-67820023 | Rare:84 | ||||
| chr14:68791050-68791313 | Common:1; Rare:66 | ||||
| chr14:68792762-68793272 | Common:3; Rare:176 |