| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24367831-24368228 | Common:2; Rare:67 | ||||
| chr14:24429855-24429974 | Rare:28 | ||||
| chr14:24442636-24443013 | Common:6; Rare:119 | ||||
| chr14:31025630-31025682 | Rare:16 | ||||
| chr14:31127912-31128233 | Common:1; Rare:58 | ||||
| chr14:31207473-31207862 | Common:2; Rare:128 | ||||
| chr14:31561291-31561475 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32432982-32433175 | Common:2; Rare:32 | ||||
| chr14:34462226-34462548 | Common:1; Rare:107 | ||||
| chr14:34539649-34539882 | Common:1; Rare:60 | ||||
| chr14:34875258-34875404 | Rare:59 | ||||
| chr14:34982504-34982680 | Common:1; Rare:72 | ||||
| chr14:35046119-35046623 | Common:2; Rare:173 | ||||
| chr14:35121950-35122761 | Common:4; Rare:228 | ||||
| chr14:35292179-35292473 | Common:5; Rare:106; Clinvar:1 |