| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23567737-23567871 | Rare:24 | ||||
| chr14:23953679-23953791 | Common:5; Rare:37 | ||||
| chr14:23988762-23988917 | Common:8; Rare:62 | ||||
| chr14:24094001-24094188 | Common:4; Rare:53 | ||||
| chr14:24114928-24115325 | Common:2; Rare:115 | ||||
| chr14:24141570-24141822 | Common:1; Rare:55 | ||||
| chr14:24146577-24146741 | Rare:56 | ||||
| chr14:24195380-24195727 | Common:2; Rare:80 | ||||
| chr14:24232276-24232698 | Common:8; Rare:108 | ||||
| chr14:24242272-24242413 | Rare:48; Clinvar (benign):1 | ||||
| chr14:24242539-24242754 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:24260374-24260942 | Common:2; Rare:177; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr14:24263522-24263590 | Common:1; Rare:11 | ||||
| chr14:24271470-24271689 | Common:2; Rare:62 | ||||
| chr14:24299676-24299884 | Common:4; Rare:61 |