| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23988772-23988917 | Common:8; Rare:59 | ||||
| chr14:24114584-24114852 | Common:1; Rare:70 | ||||
| chr14:24114998-24115286 | Common:2; Rare:80 | ||||
| chr14:24146577-24146741 | Rare:56 | ||||
| chr14:24147252-24147433 | Common:1; Rare:52 | ||||
| chr14:24195321-24195748 | Common:2; Rare:103 | ||||
| chr14:24232263-24232739 | Common:8; Rare:120 | ||||
| chr14:24242258-24242413 | Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24271460-24271611 | Common:1; Rare:45 | ||||
| chr14:24299717-24299862 | Common:4; Rare:41 | ||||
| chr14:24367878-24368206 | Common:2; Rare:56 | ||||
| chr14:24429860-24429974 | Rare:26 | ||||
| chr14:24442670-24443049 | Common:5; Rare:118 | ||||
| chr14:25049901-25050218 | Common:2; Rare:99 | ||||
| chr14:26597565-26597681 | Rare:17 |