| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23567761-23567871 | Rare:23 | ||||
| chr14:23578655-23578927 | Rare:48 | ||||
| chr14:23953667-23953784 | Common:4; Rare:38 | ||||
| chr14:23969856-23970016 | Common:8; Rare:69 | ||||
| chr14:24114478-24114852 | Common:1; Rare:88 | ||||
| chr14:24114991-24115302 | Common:2; Rare:88 | ||||
| chr14:24146564-24146683 | Rare:47 | ||||
| chr14:24171791-24172119 | Common:3; Rare:78 | ||||
| chr14:24195389-24195744 | Common:2; Rare:79 | ||||
| chr14:24232312-24232707 | Common:8; Rare:93 | ||||
| chr14:24232854-24232958 | Rare:26 | ||||
| chr14:24242571-24242747 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271485-24271639 | Common:1; Rare:41 | ||||
| chr14:24299717-24299862 | Common:4; Rare:41 | ||||
| chr14:24442659-24443019 | Common:5; Rare:117 |