| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:53953344-53953723 | Common:6; Rare:243 | ||||
| chr14:53955585-53956332 | Common:8; Rare:214 | ||||
| chr14:53956692-53957128 | Common:1; Rare:244; Clinvar:3 | ||||
| chr14:54396632-54397128 | Common:6; Rare:329 | ||||
| chr14:54440620-54441140 | Common:5; Rare:218 | ||||
| chr14:54441287-54441963 | Common:3; Rare:487 | ||||
| chr14:54488833-54489245 | Common:7; Rare:193 | ||||
| chr14:54509576-54509980 | Common:17; Rare:382 | ||||
| chr14:54566862-54567263 | Rare:160 | ||||
| chr14:54567297-54567805 | Common:7; Rare:148 | ||||
| chr14:54652260-54652670 | Rare:60 | ||||
| chr14:54901619-54902399 | Common:11; Rare:436; Clinvar:4; Clinvar (pathogenic):6 | ||||
| chr14:54902670-54902991 | Common:7; Rare:245; Clinvar:7; Clinvar (benign):10 | ||||
| chr14:55026928-55027729 | Common:11; Rare:430 | ||||
| chr14:55051287-55051804 | Common:5; Rare:498 |