| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75427643-75427792 | Rare:33 | ||||
| chr14:75660797-75661381 | Common:5; Rare:146 | ||||
| chr14:75985714-75985807 | Rare:45; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr14:77028462-77028895 | Common:1; Rare:132 | ||||
| chr14:77098001-77098364 | Rare:113 | ||||
| chr14:77320838-77321104 | Rare:82; Clinvar:1 | ||||
| chr14:77376954-77377420 | Common:5; Rare:133 | ||||
| chr14:77457550-77457878 | Common:1; Rare:97 | ||||
| chr14:77457997-77458258 | Rare:60 | ||||
| chr14:77707991-77708188 | Common:2; Rare:102 | ||||
| chr14:81220721-81221085 | Common:3; Rare:148 | ||||
| chr14:81221274-81221429 | Common:1; Rare:34 | ||||
| chr14:85530030-85530190 | Common:1; Rare:35 | ||||
| chr14:87992976-87993093 | Common:1; Rare:60; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr14:88562933-88563136 | Rare:95 |