| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73950052-73950343 | Common:6; Rare:131; Clinvar (benign):4 | ||||
| chr14:74019201-74019516 | Common:2; Rare:118 | ||||
| chr14:74084398-74084652 | Common:4; Rare:65 | ||||
| chr14:74085080-74085559 | Common:5; Rare:88 | ||||
| chr14:74302929-74303143 | Common:2; Rare:78; Clinvar (benign):1 | ||||
| chr14:74493462-74493822 | Common:3; Rare:134; Clinvar (benign):4 | ||||
| chr14:74713042-74713228 | Rare:104 | ||||
| chr14:74763124-74763414 | Rare:90 | ||||
| chr14:74881641-74882013 | Common:1; Rare:139 | ||||
| chr14:74922581-74922981 | Common:4; Rare:137 | ||||
| chr14:74923229-74923403 | Common:1; Rare:46 | ||||
| chr14:75002502-75002954 | Common:1; Rare:119; Clinvar:2 | ||||
| chr14:75051379-75051549 | Common:2; Rare:51; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:75063967-75064197 | Common:1; Rare:60 | ||||
| chr14:75069481-75069641 | Rare:42 |