| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75660794-75661055 | Rare:69 | ||||
| chr14:75661168-75661330 | Common:2; Rare:44 | ||||
| chr14:76762481-76762750 | Rare:62 | ||||
| chr14:76812849-76812992 | Rare:53 | ||||
| chr14:77028706-77028888 | Rare:57 | ||||
| chr14:77377014-77377415 | Common:4; Rare:120 | ||||
| chr14:77457539-77457877 | Common:1; Rare:101 | ||||
| chr14:77707991-77708178 | Common:2; Rare:98 | ||||
| chr14:77761112-77761262 | Rare:56 | ||||
| chr14:81220658-81221046 | Common:3; Rare:142 | ||||
| chr14:81221274-81221459 | Common:1; Rare:46 | ||||
| chr14:85530018-85530205 | Common:1; Rare:41 | ||||
| chr14:88562906-88563129 | Rare:106 | ||||
| chr14:88824325-88824710 | Common:2; Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:89954693-89954937 | Rare:66 |