| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50958478-50958834 | Common:1; Rare:122; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:51562784-51562992 | Common:3; Rare:39 | ||||
| chr20:52191672-52191868 | Rare:50 | ||||
| chr20:52972665-52972775 | Common:2; Rare:25 | ||||
| chr20:53593797-53593870 | Common:1; Rare:24 | ||||
| chr20:56392199-56392687 | Common:6; Rare:127 | ||||
| chr20:56468574-56468700 | Rare:61 | ||||
| chr20:58651073-58651305 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58651683-58652009 | Rare:74; Clinvar (benign):2 | ||||
| chr20:58888796-58888841 | Rare:16 | ||||
| chr20:58909681-58910077 | Common:1; Rare:69; Clinvar (pathogenic):2 | ||||
| chr20:58981151-58981318 | Common:2; Rare:86 | ||||
| chr20:59006410-59006673 | Common:1; Rare:74 | ||||
| chr20:59032219-59032590 | Common:3; Rare:157; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:59042741-59043022 | Common:1; Rare:108 |