| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67599781-67599859 | Common:2; Rare:17 | ||||
| chr14:67600111-67600442 | Common:8; Rare:109; Clinvar (pathogenic):1 | ||||
| chr14:67619731-67619978 | Rare:67 | ||||
| chr14:67620254-67620290 | Rare:3 | ||||
| chr14:67674197-67674349 | Common:2; Rare:38 | ||||
| chr14:67674561-67674749 | Rare:50 | ||||
| chr14:67674781-67675057 | Common:2; Rare:66 | ||||
| chr14:67695485-67695957 | Common:2; Rare:148 | ||||
| chr14:67816039-67816165 | Common:1; Rare:21 | ||||
| chr14:67816305-67816362 | Common:1; Rare:21 | ||||
| chr14:67816496-67816999 | Common:2; Rare:108; Clinvar:1 | ||||
| chr14:67819712-67819884 | Rare:44 | ||||
| chr14:67819935-67820048 | Rare:25 | ||||
| chr14:68791027-68791306 | Common:1; Rare:73 | ||||
| chr14:68791485-68791723 | Common:1; Rare:46 |