| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24195216-24195354 | Rare:40 | ||||
| chr14:24195397-24195854 | Common:3; Rare:117 | ||||
| chr14:24195945-24196077 | Common:1; Rare:30 | ||||
| chr14:24196131-24196255 | Rare:24 | ||||
| chr14:24213030-24213668 | Common:5; Rare:168 | ||||
| chr14:24215575-24215675 | Common:1; Rare:35 | ||||
| chr14:24215899-24216165 | Common:1; Rare:96 | ||||
| chr14:24232316-24232529 | Common:8; Rare:50 | ||||
| chr14:24232532-24232981 | Common:1; Rare:104 | ||||
| chr14:24242219-24242490 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:24242559-24242845 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24242942-24243156 | Common:1; Rare:39 | ||||
| chr14:24269037-24269197 | Common:1; Rare:40 | ||||
| chr14:24271122-24271314 | Rare:55 | ||||
| chr14:24271439-24271786 | Common:2; Rare:99 |