| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24114916-24115330 | Common:2; Rare:117 | ||||
| chr14:24137412-24137734 | Common:3; Rare:93 | ||||
| chr14:24141547-24141858 | Common:1; Rare:73 | ||||
| chr14:24146555-24146747 | Rare:66 | ||||
| chr14:24147258-24147532 | Common:2; Rare:79 | ||||
| chr14:24165877-24166190 | Common:1; Rare:81 | ||||
| chr14:24195316-24195756 | Common:2; Rare:108 | ||||
| chr14:24213052-24213188 | Rare:25 | ||||
| chr14:24213425-24213728 | Common:3; Rare:96 | ||||
| chr14:24232289-24232707 | Common:8; Rare:107 | ||||
| chr14:24232714-24232970 | Common:1; Rare:59 | ||||
| chr14:24235548-24235770 | Common:1; Rare:49 | ||||
| chr14:24242272-24242433 | Rare:52; Clinvar (benign):2 | ||||
| chr14:24242513-24242774 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:24271453-24271631 | Common:1; Rare:51 |