| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50116540-50116705 | Rare:77 | ||||
| chr14:50312146-50312396 | Common:1; Rare:110 | ||||
| chr14:50532518-50532798 | Common:3; Rare:88 | ||||
| chr14:50668340-50668556 | Common:3; Rare:84 | ||||
| chr14:50944480-50944578 | Common:4; Rare:27; Clinvar (benign):1 | ||||
| chr14:51240093-51240304 | Common:1; Rare:87 | ||||
| chr14:51651619-51651917 | Common:3; Rare:73 | ||||
| chr14:51989374-51989634 | Common:2; Rare:80 | ||||
| chr14:52707028-52707232 | Common:1; Rare:89 | ||||
| chr14:52729900-52730238 | Common:2; Rare:111 | ||||
| chr14:53152381-53152414 | Rare:13 | ||||
| chr14:54396681-54397065 | Common:2; Rare:109 | ||||
| chr14:54441317-54441541 | Rare:90 | ||||
| chr14:54488944-54489187 | Common:1; Rare:67 | ||||
| chr14:54509662-54509942 | Common:4; Rare:95 |