| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:88824348-88824716 | Common:2; Rare:104; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89954605-89954937 | Common:3; Rare:107 | ||||
| chr14:89955824-89955996 | Common:5; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:90331844-90332012 | Common:1; Rare:67 | ||||
| chr14:90396968-90397247 | Common:5; Rare:126; Clinvar (benign):2 | ||||
| chr14:91510161-91510367 | Rare:77 | ||||
| chr14:91510437-91510591 | Common:1; Rare:45 | ||||
| chr14:92040019-92040202 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:92121661-92122214 | Common:4; Rare:172 | ||||
| chr14:92513612-92513786 | Common:2; Rare:41 | ||||
| chr14:92793953-92794386 | Rare:140 | ||||
| chr14:93184845-93185027 | Rare:64 | ||||
| chr14:93206994-93207439 | Common:3; Rare:192 | ||||
| chr14:93332857-93332958 | Common:2; Rare:33 | ||||
| chr14:93333002-93333180 | Common:1; Rare:67 |