| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100238548-100238841 | Common:3; Rare:86 | ||||
| chr14:100375260-100375766 | Common:4; Rare:85 | ||||
| chr14:100376259-100376619 | Common:4; Rare:110 | ||||
| chr14:100476391-100476549 | Common:1; Rare:30 | ||||
| chr14:100569560-100569706 | Common:1; Rare:30 | ||||
| chr14:101809736-101809987 | Rare:52 | ||||
| chr14:101810287-101810436 | Common:2; Rare:34 | ||||
| chr14:101964368-101964670 | Common:3; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102083528-102083983 | Common:4; Rare:189 | ||||
| chr14:102086987-102087314 | Common:4; Rare:131 | ||||
| chr14:102087559-102087597 | Common:1; Rare:6 | ||||
| chr14:102139282-102139435 | Rare:70 | ||||
| chr14:102139641-102139987 | Rare:124 | ||||
| chr14:102234486-102234566 | Rare:17 | ||||
| chr14:102234973-102235058 | Rare:25 |