| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:93927138-93927352 | Rare:44 | ||||
| chr14:94081127-94081375 | Common:5; Rare:78 | ||||
| chr14:94129558-94129744 | Common:3; Rare:63 | ||||
| chr14:94390552-94390768 | Common:2; Rare:52 | ||||
| chr14:95157434-95157744 | Common:4; Rare:116 | ||||
| chr14:95534556-95534656 | Rare:43 | ||||
| chr14:96363337-96363552 | Common:1; Rare:71 | ||||
| chr14:96502301-96502580 | Common:1; Rare:122 | ||||
| chr14:99480739-99481131 | Common:2; Rare:140 | ||||
| chr14:100019414-100019596 | Rare:37 | ||||
| chr14:100238535-100238837 | Common:3; Rare:88 | ||||
| chr14:100376269-100376500 | Common:3; Rare:77 | ||||
| chr14:101809736-101809918 | Rare:40 | ||||
| chr14:101964412-101964661 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102086989-102087496 | Common:6; Rare:209 |