| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24144201-24144469 | Common:2; Rare:68 | ||||
| chr14:24146543-24146887 | Common:1; Rare:112 | ||||
| chr14:24147258-24147499 | Common:2; Rare:65 | ||||
| chr14:24195316-24195744 | Common:2; Rare:103 | ||||
| chr14:24213044-24213198 | Rare:28 | ||||
| chr14:24213425-24213626 | Common:1; Rare:68 | ||||
| chr14:24232274-24232961 | Common:9; Rare:167 | ||||
| chr14:24242264-24242407 | Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24242545-24242767 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:24267660-24267915 | Common:2; Rare:87 | ||||
| chr14:24271453-24271641 | Common:1; Rare:53 | ||||
| chr14:24299714-24299902 | Common:4; Rare:63 | ||||
| chr14:24366654-24366775 | Rare:35 | ||||
| chr14:24429836-24429996 | Common:2; Rare:39 | ||||
| chr14:24442659-24443043 | Common:5; Rare:121 |