| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50396819-50396999 | Common:3; Rare:53 | ||||
| chr14:50532455-50532773 | Common:4; Rare:100 | ||||
| chr14:50561124-50561201 | Rare:15 | ||||
| chr14:50668295-50668556 | Common:3; Rare:95 | ||||
| chr14:50944327-50944541 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51240175-51240295 | Rare:61 | ||||
| chr14:51651611-51651959 | Common:4; Rare:93 | ||||
| chr14:52004082-52004114 | Rare:13 | ||||
| chr14:52004145-52004235 | Common:1; Rare:39 | ||||
| chr14:52069008-52069232 | Common:2; Rare:45 | ||||
| chr14:52314062-52314388 | Common:3; Rare:86 | ||||
| chr14:52695496-52695812 | Common:1; Rare:87 | ||||
| chr14:52707028-52707247 | Common:1; Rare:95 | ||||
| chr14:52791447-52791757 | Common:1; Rare:108 | ||||
| chr14:52951211-52951436 | Common:3; Rare:92 |