| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50396874-50396991 | Common:1; Rare:31 | ||||
| chr14:50532442-50532781 | Common:4; Rare:110 | ||||
| chr14:50668334-50668556 | Common:3; Rare:84 | ||||
| chr14:50944379-50944590 | Common:4; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51240132-51240305 | Rare:79 | ||||
| chr14:51651448-51651460 | Rare:4 | ||||
| chr14:51651619-51651971 | Common:4; Rare:96 | ||||
| chr14:51860557-51860781 | Rare:64 | ||||
| chr14:51999467-51999749 | Common:1; Rare:55 | ||||
| chr14:52004076-52004221 | Common:1; Rare:59 | ||||
| chr14:52068990-52069215 | Common:2; Rare:53 | ||||
| chr14:52314191-52314333 | Rare:47 | ||||
| chr14:52707088-52707307 | Common:1; Rare:81 | ||||
| chr14:52729856-52730243 | Common:2; Rare:121 | ||||
| chr14:52791418-52791757 | Common:1; Rare:113 |