| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77760653-77760812 | Common:1; Rare:70 | ||||
| chr14:77760973-77761269 | Rare:111 | ||||
| chr14:77799968-77800233 | Common:1; Rare:59 | ||||
| chr14:77800274-77800566 | Common:1; Rare:51 | ||||
| chr14:79279103-79279449 | Common:3; Rare:80 | ||||
| chr14:79279896-79279928 | Rare:8 | ||||
| chr14:80941633-80941908 | Common:2; Rare:65 | ||||
| chr14:81220800-81221582 | Common:3; Rare:281 | ||||
| chr14:81324093-81324302 | Common:1; Rare:33 | ||||
| chr14:81436044-81436307 | Common:3; Rare:80 | ||||
| chr14:81436401-81436651 | Common:4; Rare:94 | ||||
| chr14:81533769-81534007 | Common:1; Rare:68 | ||||
| chr14:87992808-87992876 | Rare:15 | ||||
| chr14:87992914-87993362 | Common:6; Rare:203; Clinvar:16; Clinvar (benign):10; Clinvar (pathogenic):9 | ||||
| chr14:87993485-87993516 | Rare:12; Clinvar:1 |