| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24232308-24232707 | Common:8; Rare:94 | ||||
| chr14:24242295-24242433 | Rare:46; Clinvar (benign):1 | ||||
| chr14:24242604-24242774 | Rare:40; Clinvar:1 | ||||
| chr14:30622151-30622353 | Rare:69 | ||||
| chr14:31025441-31025647 | Common:2; Rare:45 | ||||
| chr14:31207618-31207946 | Common:2; Rare:114 | ||||
| chr14:31420528-31420913 | Common:4; Rare:103 | ||||
| chr14:32076685-32077041 | Common:3; Rare:109 | ||||
| chr14:34462224-34462530 | Common:1; Rare:103 | ||||
| chr14:34539619-34539875 | Common:1; Rare:73 | ||||
| chr14:34875302-34875417 | Rare:43 | ||||
| chr14:35046105-35046531 | Common:2; Rare:145 | ||||
| chr14:35121955-35122628 | Common:3; Rare:192 | ||||
| chr14:35292179-35292462 | Common:4; Rare:102 | ||||
| chr14:39175022-39175272 | Common:3; Rare:87 |