| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:34982373-34982696 | Common:1; Rare:129 | ||||
| chr14:35046130-35046550 | Common:1; Rare:144 | ||||
| chr14:35122265-35122695 | Common:2; Rare:123 | ||||
| chr14:35292232-35292479 | Common:4; Rare:93; Clinvar:1 | ||||
| chr14:35402765-35403160 | Common:4; Rare:115; Clinvar (benign):4 | ||||
| chr14:37197865-37198103 | Common:3; Rare:74 | ||||
| chr14:39170249-39170454 | Common:3; Rare:54 | ||||
| chr14:39432431-39432618 | Common:6; Rare:60 | ||||
| chr14:41606842-41607118 | Common:4; Rare:83 | ||||
| chr14:44961855-44962278 | Common:3; Rare:129 | ||||
| chr14:45253150-45253312 | Rare:40 | ||||
| chr14:49586298-49586776 | Common:1; Rare:246; Clinvar (benign):1 | ||||
| chr14:49598723-49599014 | Common:2; Rare:107 | ||||
| chr14:49620561-49620837 | Common:2; Rare:114; Clinvar:3 | ||||
| chr14:49892897-49893118 | Rare:90 |