| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:69152968-69153324 | Rare:141 | ||||
| chr14:69191410-69191606 | Rare:66 | ||||
| chr14:69191745-69191881 | Rare:31 | ||||
| chr14:69398232-69398742 | Common:3; Rare:275 | ||||
| chr14:69611375-69611759 | Common:2; Rare:222 | ||||
| chr14:69767510-69767930 | Common:4; Rare:264 | ||||
| chr14:69879217-69879491 | Common:8; Rare:154 | ||||
| chr14:69879609-69879832 | Common:1; Rare:68; Clinvar:1 | ||||
| chr14:69951851-69952337 | Common:6; Rare:167; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr14:70359535-70359960 | Common:2; Rare:144 | ||||
| chr14:70416977-70417156 | Rare:94 | ||||
| chr14:70600619-70600942 | Common:6; Rare:147 | ||||
| chr14:70809420-70809990 | Common:10; Rare:303 | ||||
| chr14:70907312-70907929 | Common:8; Rare:217 | ||||
| chr14:71320260-71320512 | Rare:141 |