| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24429852-24429980 | Rare:31 | ||||
| chr14:24442650-24443043 | Common:5; Rare:123 | ||||
| chr14:25049890-25050216 | Common:3; Rare:99 | ||||
| chr14:26597438-26597627 | Common:1; Rare:36 | ||||
| chr14:30559048-30559235 | Common:2; Rare:71 | ||||
| chr14:30622221-30622369 | Common:1; Rare:71 | ||||
| chr14:31025322-31025673 | Common:2; Rare:79 | ||||
| chr14:31026831-31026966 | Common:1; Rare:34 | ||||
| chr14:31101203-31101470 | Rare:61 | ||||
| chr14:31207473-31207849 | Common:2; Rare:125 | ||||
| chr14:31208137-31208222 | Common:1; Rare:23 | ||||
| chr14:31420503-31420770 | Common:4; Rare:86 | ||||
| chr14:31457365-31457577 | Common:2; Rare:75 | ||||
| chr14:31561089-31561465 | Common:4; Rare:102; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32075739-32075899 | Rare:32 |