| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49892653-49892732 | Common:3; Rare:19 | ||||
| chr14:49892813-49893173 | Common:1; Rare:156 | ||||
| chr14:49893180-49893461 | Common:2; Rare:82 | ||||
| chr14:49893481-49893553 | Common:2; Rare:16 | ||||
| chr14:50116487-50116766 | Common:1; Rare:143 | ||||
| chr14:50230893-50231256 | Common:4; Rare:102; Clinvar (benign):1 | ||||
| chr14:50231526-50231686 | Common:1; Rare:46 | ||||
| chr14:50231688-50231806 | Rare:33 | ||||
| chr14:50231837-50232067 | Common:1; Rare:91 | ||||
| chr14:50311872-50312079 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:50312094-50312430 | Common:2; Rare:142; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:50312469-50312756 | Common:9; Rare:97 | ||||
| chr14:50312917-50312946 | Rare:6 | ||||
| chr14:50396328-50396656 | Common:3; Rare:70 | ||||
| chr14:50396743-50396956 | Common:4; Rare:61 |