| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31420447-31420811 | Common:6; Rare:118 | ||||
| chr14:31456841-31457031 | Common:1; Rare:28 | ||||
| chr14:31457034-31457339 | Common:2; Rare:91 | ||||
| chr14:31457356-31457638 | Common:2; Rare:90 | ||||
| chr14:31561085-31561701 | Common:4; Rare:163; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:32075825-32076018 | Rare:41 | ||||
| chr14:32076090-32076356 | Common:2; Rare:69 | ||||
| chr14:32076416-32077154 | Common:3; Rare:194 | ||||
| chr14:32077228-32077425 | Rare:58 | ||||
| chr14:32077444-32077631 | Common:1; Rare:67 | ||||
| chr14:32077757-32078276 | Common:1; Rare:135 | ||||
| chr14:32473613-32473855 | Common:3; Rare:49 | ||||
| chr14:32938706-32938956 | Common:2; Rare:87 | ||||
| chr14:32939171-32939686 | Common:2; Rare:116 | ||||
| chr14:32939719-32939924 | Rare:52 |