| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50668327-50668562 | Common:4; Rare:89 | ||||
| chr14:50944336-50944583 | Common:4; Rare:92; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51095047-51095297 | Common:4; Rare:94 | ||||
| chr14:51240093-51240295 | Common:1; Rare:81 | ||||
| chr14:51651601-51651990 | Common:4; Rare:106 | ||||
| chr14:51989374-51989642 | Common:2; Rare:86 | ||||
| chr14:52003917-52004227 | Common:2; Rare:101 | ||||
| chr14:52069000-52069215 | Common:2; Rare:49 | ||||
| chr14:52314209-52314319 | Rare:37 | ||||
| chr14:52791447-52791792 | Common:2; Rare:118 | ||||
| chr14:52950937-52951461 | Common:4; Rare:183 | ||||
| chr14:53153227-53153396 | Common:2; Rare:67 | ||||
| chr14:54567035-54567177 | Rare:40 | ||||
| chr14:55027085-55027295 | Common:2; Rare:58 | ||||
| chr14:55051479-55051742 | Rare:115 |