| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75427599-75427693 | Rare:30 | ||||
| chr14:75427707-75427770 | Rare:14 | ||||
| chr14:75660834-75661064 | Rare:62 | ||||
| chr14:75661189-75661314 | Common:2; Rare:36 | ||||
| chr14:75985709-75985798 | Rare:42; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr14:76151788-76151962 | Rare:58 | ||||
| chr14:76762653-76762839 | Rare:56 | ||||
| chr14:77320838-77321091 | Rare:78; Clinvar:1 | ||||
| chr14:77377046-77377398 | Common:2; Rare:97 | ||||
| chr14:77457550-77457876 | Common:1; Rare:97 | ||||
| chr14:77707991-77708201 | Common:2; Rare:107 | ||||
| chr14:77761129-77761203 | Rare:37 | ||||
| chr14:81220859-81221046 | Common:1; Rare:92 | ||||
| chr14:89954716-89954935 | Rare:57 | ||||
| chr14:90396973-90397232 | Common:5; Rare:121; Clinvar (benign):2 |