| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:89954661-89954972 | Rare:162 | ||||
| chr14:89955797-89955997 | Common:9; Rare:70; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:90256477-90256603 | Common:4; Rare:80 | ||||
| chr14:90331918-90332188 | Common:2; Rare:138 | ||||
| chr14:90396870-90397161 | Common:6; Rare:230 | ||||
| chr14:91060570-91060900 | Common:2; Rare:97 | ||||
| chr14:91113997-91114709 | Common:5; Rare:223 | ||||
| chr14:91417759-91418216 | Common:5; Rare:166 | ||||
| chr14:91508920-91509330 | Common:4; Rare:154 | ||||
| chr14:91510215-91510655 | Common:2; Rare:262 | ||||
| chr14:92040023-92040192 | Common:4; Rare:87; Clinvar (benign):2 | ||||
| chr14:92106554-92106796 | Common:4; Rare:159 | ||||
| chr14:92121652-92122014 | Common:10; Rare:241 | ||||
| chr14:92513489-92513841 | Common:3; Rare:129 | ||||
| chr14:92748616-92748781 | Rare:44 |