| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35826300-35826427 | Rare:30 | ||||
| chr14:44961892-44962258 | Common:3; Rare:106 | ||||
| chr14:49598694-49599018 | Common:2; Rare:123 | ||||
| chr14:49620575-49620817 | Common:2; Rare:95; Clinvar:1 | ||||
| chr14:50312165-50312376 | Rare:92 | ||||
| chr14:50944323-50944578 | Common:4; Rare:97; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51240016-51240295 | Common:2; Rare:98 | ||||
| chr14:51651662-51652013 | Common:4; Rare:101 | ||||
| chr14:52552498-52552863 | Common:1; Rare:110 | ||||
| chr14:52791466-52791756 | Common:1; Rare:101 | ||||
| chr14:52951011-52951442 | Common:4; Rare:153 | ||||
| chr14:54567024-54567154 | Rare:37 | ||||
| chr14:55027049-55027334 | Common:2; Rare:79 | ||||
| chr14:55191538-55191721 | Common:4; Rare:42 | ||||
| chr14:55580080-55580294 | Common:2; Rare:93 |