| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50312498-50312764 | Common:22; Rare:233 | ||||
| chr14:50532436-50533098 | Common:15; Rare:419 | ||||
| chr14:50559840-50560292 | Rare:194 | ||||
| chr14:50561029-50561350 | Common:1; Rare:100 | ||||
| chr14:50667785-50667947 | Rare:70 | ||||
| chr14:50668145-50668869 | Common:31; Rare:649 | ||||
| chr14:50830612-50830858 | Common:2; Rare:60 | ||||
| chr14:50831060-50831394 | Common:3; Rare:250 | ||||
| chr14:50944364-50944626 | Common:9; Rare:215; Clinvar:3; Clinvar (benign):6 | ||||
| chr14:50944690-50945120 | Common:7; Rare:157 | ||||
| chr14:51094940-51095490 | Common:9; Rare:297 | ||||
| chr14:51239950-51240334 | Common:4; Rare:244 | ||||
| chr14:51564940-51565350 | Rare:129 | ||||
| chr14:51651304-51652153 | Common:18; Rare:550 | ||||
| chr14:51860401-51860801 | Rare:190 |