| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:51651601-51651917 | Common:3; Rare:74 | ||||
| chr14:51989376-51989642 | Common:2; Rare:85 | ||||
| chr14:52003940-52004227 | Common:2; Rare:93 | ||||
| chr14:52707040-52707298 | Common:1; Rare:105 | ||||
| chr14:52791418-52791785 | Common:2; Rare:119 | ||||
| chr14:52950997-52951418 | Common:4; Rare:148 | ||||
| chr14:53152359-53152424 | Rare:26 | ||||
| chr14:53956814-53956993 | Rare:43 | ||||
| chr14:54902819-54902962 | Rare:40; Clinvar (benign):1 | ||||
| chr14:55027035-55027290 | Common:2; Rare:72 | ||||
| chr14:55051470-55051748 | Rare:123 | ||||
| chr14:55191513-55191747 | Common:5; Rare:53 | ||||
| chr14:55580096-55580331 | Common:2; Rare:102 | ||||
| chr14:57268526-57268622 | Rare:26 | ||||
| chr14:57268664-57269113 | Common:2; Rare:139 |