| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:68836336-68836524 | Rare:23 | ||||
| chr14:68925348-68925672 | Common:1; Rare:57 | ||||
| chr14:68937949-68938160 | Common:1; Rare:33 | ||||
| chr14:69209849-69210059 | Common:1; Rare:40 | ||||
| chr14:70010032-70010206 | Rare:35 | ||||
| chr14:70973289-70973517 | Rare:33 | ||||
| chr14:70988838-70988979 | Rare:19 | ||||
| chr14:71086776-71086947 | Common:1; Rare:37 | ||||
| chr14:71109522-71109951 | Common:1; Rare:107 | ||||
| chr14:71143238-71143517 | Common:1; Rare:51 | ||||
| chr14:71322146-71322273 | Common:1; Rare:29 | ||||
| chr14:73130900-73130916 | Rare:3 | ||||
| chr14:73186818-73186885 | Rare:12; Clinvar (pathogenic):2 | ||||
| chr14:73245951-73246129 | Common:2; Rare:77 | ||||
| chr14:73274809-73274840 | Rare:6 |