| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50504499-50504802 | Common:1; Rare:64 | ||||
| chr14:50532423-50532798 | Common:4; Rare:117 | ||||
| chr14:50561080-50561255 | Rare:29 | ||||
| chr14:50667894-50668160 | Rare:107 | ||||
| chr14:50668288-50668557 | Common:4; Rare:96 | ||||
| chr14:50944327-50944540 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51095125-51095297 | Common:3; Rare:67 | ||||
| chr14:51240096-51240305 | Common:1; Rare:88 | ||||
| chr14:51651448-51651505 | Rare:22 | ||||
| chr14:51651620-51651990 | Common:4; Rare:105 | ||||
| chr14:51989368-51989670 | Common:2; Rare:96 | ||||
| chr14:51999549-51999796 | Common:1; Rare:52 | ||||
| chr14:52004107-52004239 | Common:1; Rare:52 | ||||
| chr14:52068842-52069247 | Common:3; Rare:121 | ||||
| chr14:52267573-52267729 | Common:2; Rare:51 |