| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:92039937-92040901 | Common:14; Rare:376; Clinvar:12; Clinvar (benign):6 | ||||
| chr14:92040808-92041009 | Common:1; Rare:55 | ||||
| chr14:92105540-92106104 | Common:7; Rare:164 | ||||
| chr14:92106110-92106500 | Common:1; Rare:165 | ||||
| chr14:92106509-92106849 | Common:5; Rare:178 | ||||
| chr14:92121359-92121514 | Common:4; Rare:27 | ||||
| chr14:92121619-92122290 | Common:15; Rare:582 | ||||
| chr14:92513560-92513688 | Common:2; Rare:30 | ||||
| chr14:92513609-92513793 | Common:2; Rare:42 | ||||
| chr14:92748488-92748850 | Rare:148 | ||||
| chr14:92793875-92794468 | Rare:463 | ||||
| chr14:92926373-92926864 | Common:3; Rare:139 | ||||
| chr14:93037210-93037560 | Rare:105 | ||||
| chr14:93115080-93116127 | Common:13; Rare:714 | ||||
| chr14:93184205-93184519 | Common:4; Rare:101 |