| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77457529-77457886 | Common:2; Rare:108 | ||||
| chr14:77458007-77458200 | Rare:53 | ||||
| chr14:77616801-77617126 | Common:1; Rare:70 | ||||
| chr14:77708000-77708209 | Common:2; Rare:105 | ||||
| chr14:77761113-77761203 | Rare:43 | ||||
| chr14:77800011-77800145 | Rare:22 | ||||
| chr14:80941694-80941945 | Common:3; Rare:58 | ||||
| chr14:81220855-81221069 | Common:1; Rare:102 | ||||
| chr14:81221231-81221549 | Common:1; Rare:94 | ||||
| chr14:85530033-85530184 | Common:1; Rare:34 | ||||
| chr14:87992988-87993314 | Common:5; Rare:152; Clinvar:14; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr14:88562946-88563094 | Rare:70 | ||||
| chr14:89619085-89619299 | Common:1; Rare:75 | ||||
| chr14:89954548-89954950 | Common:3; Rare:138 | ||||
| chr14:89956440-89956556 | Common:1; Rare:29 |