| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:36320531-36320764 | Common:4; Rare:80 | ||||
| chr14:37197880-37198093 | Common:2; Rare:66 | ||||
| chr14:39174907-39175296 | Common:6; Rare:138 | ||||
| chr14:39266965-39267414 | Common:3; Rare:148 | ||||
| chr14:39432447-39432618 | Common:6; Rare:59 | ||||
| chr14:44961882-44962278 | Common:3; Rare:117 | ||||
| chr14:45253078-45253316 | Rare:64 | ||||
| chr14:49586335-49586778 | Common:1; Rare:239 | ||||
| chr14:49598684-49599014 | Common:2; Rare:126 | ||||
| chr14:49620562-49620835 | Common:2; Rare:113; Clinvar:3 | ||||
| chr14:49693022-49693154 | Rare:38 | ||||
| chr14:49768447-49768540 | Rare:40 | ||||
| chr14:49892913-49893231 | Rare:119 | ||||
| chr14:50312081-50312376 | Common:1; Rare:126; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:50532488-50532643 | Common:2; Rare:44 |