| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100238540-100238831 | Common:3; Rare:85 | ||||
| chr14:100376264-100376526 | Common:3; Rare:85 | ||||
| chr14:101809706-101809890 | Rare:39 | ||||
| chr14:101810264-101810372 | Rare:21 | ||||
| chr14:101964359-101964595 | Common:2; Rare:67; Clinvar:1 | ||||
| chr14:102086987-102087480 | Common:6; Rare:209 | ||||
| chr14:102139650-102139932 | Rare:99 | ||||
| chr14:102316901-102317113 | Common:4; Rare:94 | ||||
| chr14:102362849-102363092 | Rare:111 | ||||
| chr14:103333898-103334252 | Common:3; Rare:147 | ||||
| chr14:103529058-103529244 | Common:1; Rare:54 | ||||
| chr14:103562624-103563104 | Common:8; Rare:193; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:103715437-103715833 | Common:1; Rare:129 | ||||
| chr14:103921480-103921711 | Common:3; Rare:75 | ||||
| chr14:104752841-104753234 | Common:3; Rare:136 |