| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24429861-24429930 | Rare:19 | ||||
| chr14:24442636-24443013 | Common:6; Rare:119 | ||||
| chr14:26596562-26596734 | Rare:33 | ||||
| chr14:26596807-26596924 | Common:1; Rare:26 | ||||
| chr14:26597303-26597954 | Common:3; Rare:146 | ||||
| chr14:28765211-28765391 | Common:1; Rare:31 | ||||
| chr14:30559047-30559221 | Common:2; Rare:67 | ||||
| chr14:30622174-30622391 | Common:1; Rare:100 | ||||
| chr14:31025136-31025664 | Common:2; Rare:125 | ||||
| chr14:31207618-31207906 | Common:2; Rare:100 | ||||
| chr14:31208137-31208235 | Common:1; Rare:27 | ||||
| chr14:31420511-31420763 | Common:3; Rare:79 | ||||
| chr14:31457350-31457577 | Common:2; Rare:80 | ||||
| chr14:31561328-31561547 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:32075651-32075884 | Common:1; Rare:47 |