| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49800502-49800828 | Common:1; Rare:87 | ||||
| chr14:49892909-49893154 | Rare:101 | ||||
| chr14:50312146-50312380 | Rare:104 | ||||
| chr14:50396863-50396999 | Common:2; Rare:36 | ||||
| chr14:50532461-50532782 | Common:4; Rare:104 | ||||
| chr14:50561124-50561273 | Common:1; Rare:23 | ||||
| chr14:50668295-50668556 | Common:3; Rare:95 | ||||
| chr14:50831035-50831260 | Common:1; Rare:78 | ||||
| chr14:50944342-50944661 | Common:6; Rare:109; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51240154-51240301 | Rare:68 | ||||
| chr14:51651620-51651962 | Common:4; Rare:95 | ||||
| chr14:52004003-52004239 | Common:1; Rare:82 | ||||
| chr14:52068996-52069215 | Common:2; Rare:51 | ||||
| chr14:52267587-52267735 | Common:2; Rare:51 | ||||
| chr14:52314108-52314388 | Common:2; Rare:76 |