| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:94390578-94390790 | Common:1; Rare:56 | ||||
| chr14:95157424-95157744 | Common:4; Rare:118 | ||||
| chr14:95534609-95534672 | Rare:16 | ||||
| chr14:95534769-95535050 | Common:4; Rare:85; Clinvar (benign):1 | ||||
| chr14:96363276-96363552 | Common:1; Rare:91 | ||||
| chr14:96502327-96502471 | Rare:60 | ||||
| chr14:99480786-99481007 | Common:2; Rare:87 | ||||
| chr14:100238558-100238790 | Common:2; Rare:71 | ||||
| chr14:100239523-100239559 | Rare:9 | ||||
| chr14:100376268-100376495 | Common:3; Rare:77 | ||||
| chr14:101964213-101964670 | Common:5; Rare:122; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102086990-102087330 | Common:4; Rare:138 | ||||
| chr14:102139670-102139939 | Rare:92 | ||||
| chr14:102362847-102363094 | Rare:112 | ||||
| chr14:103333957-103334258 | Common:1; Rare:125 |