| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100239543-100239584 | Rare:13 | ||||
| chr14:100239643-100239915 | Common:2; Rare:101 | ||||
| chr14:100375429-100375758 | Common:2; Rare:51 | ||||
| chr14:100376259-100376511 | Common:3; Rare:80 | ||||
| chr14:101823788-101823806 | Rare:1 | ||||
| chr14:101964393-101964670 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102087550-102087622 | Common:1; Rare:20 | ||||
| chr14:102139663-102139926 | Rare:92 | ||||
| chr14:102362843-102363103 | Rare:116 | ||||
| chr14:103333924-103334254 | Common:3; Rare:140 | ||||
| chr14:103385538-103385863 | Common:1; Rare:74 | ||||
| chr14:103519911-103520246 | Common:1; Rare:101 | ||||
| chr14:103521089-103521186 | Common:1; Rare:30 | ||||
| chr14:103529070-103529258 | Common:1; Rare:58 | ||||
| chr14:103562282-103562471 | Common:1; Rare:76 |