| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35046130-35046586 | Common:1; Rare:156 | ||||
| chr14:35122480-35122751 | Common:2; Rare:86 | ||||
| chr14:35402381-35403292 | Common:6; Rare:281; Clinvar:5; Clinvar (benign):6 | ||||
| chr14:35826292-35826444 | Rare:38 | ||||
| chr14:36320584-36320766 | Common:3; Rare:58 | ||||
| chr14:37197865-37198048 | Common:2; Rare:57 | ||||
| chr14:39114137-39114356 | Common:2; Rare:76 | ||||
| chr14:39267075-39267396 | Common:1; Rare:107 | ||||
| chr14:44961908-44962244 | Common:3; Rare:97 | ||||
| chr14:45253088-45253301 | Rare:56 | ||||
| chr14:45253522-45253612 | Common:1; Rare:37 | ||||
| chr14:49586347-49586772 | Common:1; Rare:227 | ||||
| chr14:49598725-49599014 | Common:1; Rare:106 | ||||
| chr14:49620564-49620820 | Common:2; Rare:103; Clinvar:1 | ||||
| chr14:49892932-49893154 | Rare:90 |