| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:53954042-53954269 | Common:1; Rare:49 | ||||
| chr14:53954472-53954660 | Rare:30 | ||||
| chr14:54396643-54397108 | Common:2; Rare:121 | ||||
| chr14:54488456-54488542 | Common:1; Rare:24 | ||||
| chr14:54488591-54489099 | Common:3; Rare:143 | ||||
| chr14:54509423-54509585 | Rare:28 | ||||
| chr14:54509598-54509979 | Common:6; Rare:135 | ||||
| chr14:54510257-54510348 | Rare:13 | ||||
| chr14:54566624-54566818 | Rare:53 | ||||
| chr14:54566828-54567199 | Common:1; Rare:97 | ||||
| chr14:54567481-54567776 | Common:2; Rare:59 | ||||
| chr14:54568041-54568229 | Common:1; Rare:45 | ||||
| chr14:54652218-54652511 | Rare:48 | ||||
| chr14:54902117-54902399 | Common:2; Rare:96; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr14:54902679-54902867 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):4 |