| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50532455-50532798 | Common:4; Rare:106 | ||||
| chr14:50668295-50668560 | Common:4; Rare:98 | ||||
| chr14:50944378-50944550 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51095130-51095396 | Common:3; Rare:111 | ||||
| chr14:51240124-51240305 | Rare:82 | ||||
| chr14:51651600-51651984 | Common:4; Rare:104 | ||||
| chr14:51989368-51989700 | Common:2; Rare:108 | ||||
| chr14:51999467-51999796 | Common:2; Rare:66 | ||||
| chr14:52003968-52004227 | Common:1; Rare:86 | ||||
| chr14:52068986-52069232 | Common:2; Rare:57 | ||||
| chr14:52314073-52314619 | Common:4; Rare:154 | ||||
| chr14:52552470-52552823 | Common:1; Rare:109 | ||||
| chr14:52707058-52707339 | Common:1; Rare:106 | ||||
| chr14:52791203-52791217 | Rare:3 | ||||
| chr14:52791427-52791757 | Common:1; Rare:111 |