| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74713065-74713205 | Rare:74 | ||||
| chr14:74763243-74763414 | Rare:62 | ||||
| chr14:74881779-74881973 | Common:1; Rare:90 | ||||
| chr14:75002726-75003017 | Common:1; Rare:101; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr14:75127008-75127090 | Rare:24 | ||||
| chr14:75578382-75578630 | Common:2; Rare:44; Clinvar (benign):1 | ||||
| chr14:75660789-75660948 | Rare:40 | ||||
| chr14:75661175-75661314 | Common:2; Rare:40 | ||||
| chr14:77320859-77321104 | Rare:74; Clinvar:1 | ||||
| chr14:77376969-77377412 | Common:5; Rare:127 | ||||
| chr14:77457542-77458145 | Common:2; Rare:167 | ||||
| chr14:77707992-77708180 | Common:2; Rare:99 | ||||
| chr14:77761129-77761306 | Common:2; Rare:61 | ||||
| chr14:80941700-80941978 | Common:4; Rare:69 | ||||
| chr14:81220867-81221046 | Common:1; Rare:86 |