| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50115908-50116089 | Common:2; Rare:47 | ||||
| chr20:50190572-50190939 | Rare:99 | ||||
| chr20:50191174-50191658 | Common:2; Rare:151 | ||||
| chr20:50636886-50637091 | Common:2; Rare:38 | ||||
| chr20:50930306-50930518 | Common:2; Rare:70 | ||||
| chr20:50945682-50945907 | Rare:57; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr20:50958467-50958863 | Common:1; Rare:148; Clinvar:2; Clinvar (benign):4 | ||||
| chr20:51562832-51563068 | Common:1; Rare:37 | ||||
| chr20:56359071-56359184 | Rare:30 | ||||
| chr20:56392145-56392744 | Common:6; Rare:163 | ||||
| chr20:56392780-56392959 | Common:1; Rare:43 | ||||
| chr20:56411877-56412265 | Common:4; Rare:61 | ||||
| chr20:56412285-56412331 | Rare:7 | ||||
| chr20:56468341-56468797 | Rare:139 | ||||
| chr20:58438781-58438972 | Common:1; Rare:38; Clinvar:1 |