| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75126983-75127082 | Rare:38 | ||||
| chr14:75176376-75176472 | Rare:20 | ||||
| chr14:75176514-75176922 | Common:1; Rare:111 | ||||
| chr14:75278271-75278546 | Common:2; Rare:56 | ||||
| chr14:75278913-75279121 | Common:1; Rare:66 | ||||
| chr14:75427913-75428226 | Rare:72 | ||||
| chr14:75660827-75661631 | Common:8; Rare:198 | ||||
| chr14:77097925-77098399 | Rare:150 | ||||
| chr14:77320817-77321120 | Rare:99; Clinvar:3 | ||||
| chr14:77377073-77377431 | Common:1; Rare:105 | ||||
| chr14:77457496-77458269 | Common:2; Rare:209 | ||||
| chr14:77468112-77468519 | Common:4; Rare:91 | ||||
| chr14:77616628-77616779 | Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:77707994-77708155 | Common:2; Rare:89 | ||||
| chr14:77760265-77760557 | Common:4; Rare:60 |