| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:67241117-67241574 | Common:1; Rare:114 | ||||
| chr14:67359661-67360030 | Common:1; Rare:132 | ||||
| chr14:67360245-67360435 | Common:2; Rare:56 | ||||
| chr14:67600195-67600370 | Common:4; Rare:68; Clinvar (pathogenic):1 | ||||
| chr14:67674375-67674420 | Common:1; Rare:14 | ||||
| chr14:67816563-67816751 | Rare:35; Clinvar:1 | ||||
| chr14:68793088-68793228 | Rare:29 | ||||
| chr14:68794588-68794750 | Rare:45 | ||||
| chr14:68796074-68796123 | Rare:25 | ||||
| chr14:68978957-68979401 | Common:3; Rare:115 | ||||
| chr14:68979438-68979554 | Rare:39 | ||||
| chr14:69191421-69191582 | Rare:36 | ||||
| chr14:69398234-69398448 | Common:1; Rare:83 | ||||
| chr14:69398576-69398938 | Rare:81 | ||||
| chr14:69399067-69399245 | Rare:27 |