| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:88563327-88563727 | Rare:163; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:88792785-88793077 | Rare:88 | ||||
| chr14:88824316-88824708 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:89417103-89417319 | Rare:56 | ||||
| chr14:89619119-89619307 | Common:1; Rare:67 | ||||
| chr14:89954600-89955010 | Common:3; Rare:127 | ||||
| chr14:89955806-89956012 | Common:9; Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:90256463-90256595 | Common:2; Rare:45 | ||||
| chr14:90331608-90331720 | Rare:34 | ||||
| chr14:90331908-90332235 | Common:1; Rare:97 | ||||
| chr14:90396830-90397106 | Common:4; Rare:145 | ||||
| chr14:90400910-90401310 | Common:1; Rare:88; Clinvar (benign):2 | ||||
| chr14:91060560-91061070 | Common:3; Rare:143 | ||||
| chr14:91114002-91114147 | Rare:46 | ||||
| chr14:91114274-91114428 | Rare:30 |