| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23408205-23408585 | Common:2; Rare:84; Clinvar (benign):3 | ||||
| chr14:23435631-23435991 | Common:2; Rare:69 | ||||
| chr14:23469547-23469727 | Common:1; Rare:41 | ||||
| chr14:23555941-23556087 | Common:1; Rare:41 | ||||
| chr14:23556208-23556268 | Common:1; Rare:14 | ||||
| chr14:23567468-23567550 | Rare:23 | ||||
| chr14:23953661-23953810 | Common:6; Rare:53 | ||||
| chr14:23969859-23969982 | Common:4; Rare:59 | ||||
| chr14:23988770-23988929 | Common:8; Rare:65 | ||||
| chr14:24094013-24094313 | Common:3; Rare:79 | ||||
| chr14:24114896-24115338 | Common:3; Rare:123 | ||||
| chr14:24136062-24136422 | Common:2; Rare:115 | ||||
| chr14:24141562-24141862 | Common:1; Rare:67 | ||||
| chr14:24146532-24146882 | Common:1; Rare:115 | ||||
| chr14:24147263-24147622 | Common:4; Rare:88 |