| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24237006-24237300 | Common:1; Rare:91 | ||||
| chr14:24242272-24242430 | Rare:51; Clinvar (benign):2 | ||||
| chr14:24242559-24242758 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271457-24271611 | Common:1; Rare:46 | ||||
| chr14:24299717-24299862 | Common:4; Rare:41 | ||||
| chr14:24367911-24368222 | Common:2; Rare:51 | ||||
| chr14:24429666-24429980 | Common:2; Rare:82 | ||||
| chr14:24442650-24443013 | Common:5; Rare:118 | ||||
| chr14:26597432-26597628 | Common:1; Rare:36 | ||||
| chr14:30622190-30622353 | Rare:60 | ||||
| chr14:31025432-31025673 | Common:2; Rare:54 | ||||
| chr14:31026370-31026663 | Common:4; Rare:92 | ||||
| chr14:31207465-31207862 | Common:2; Rare:131 | ||||
| chr14:31561089-31561450 | Common:4; Rare:97; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32075953-32076336 | Common:2; Rare:100 |