| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50312155-50312374 | Rare:93 | ||||
| chr14:50396879-50396991 | Common:1; Rare:28 | ||||
| chr14:50532512-50532624 | Common:2; Rare:32 | ||||
| chr14:50668295-50668556 | Common:3; Rare:95 | ||||
| chr14:50944405-50944556 | Common:3; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51095089-51095396 | Common:4; Rare:131 | ||||
| chr14:51240111-51240305 | Common:1; Rare:86 | ||||
| chr14:51651627-51651993 | Common:4; Rare:105 | ||||
| chr14:52003985-52004221 | Common:1; Rare:82 | ||||
| chr14:52069000-52069226 | Common:2; Rare:50 | ||||
| chr14:52314108-52314324 | Common:1; Rare:58 | ||||
| chr14:52552488-52552886 | Common:1; Rare:121 | ||||
| chr14:52707057-52707261 | Common:1; Rare:93 | ||||
| chr14:52791452-52791792 | Common:2; Rare:116 | ||||
| chr14:52951003-52951395 | Common:4; Rare:139 |