| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:53593776-53593914 | Common:1; Rare:51 | ||||
| chr20:56392187-56392683 | Common:6; Rare:129 | ||||
| chr20:57560802-57561226 | Common:1; Rare:78; Clinvar:1 | ||||
| chr20:57563000-57563410 | Common:2; Rare:124; Clinvar (benign):1 | ||||
| chr20:58309418-58309715 | Common:2; Rare:117 | ||||
| chr20:58651150-58651305 | Common:2; Rare:31; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58651477-58651907 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):4 | ||||
| chr20:58651946-58652148 | Rare:62; Clinvar (benign):1 | ||||
| chr20:58981144-58981326 | Common:2; Rare:89 | ||||
| chr20:59006389-59006631 | Rare:74 | ||||
| chr20:59032219-59032374 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:59836133-59836431 | Common:3; Rare:55 | ||||
| chr20:59940238-59940494 | Rare:101 | ||||
| chr20:62143299-62143835 | Common:6; Rare:231 | ||||
| chr20:62182932-62183048 | Rare:34 |