| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58651592-58651913 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):3 | ||||
| chr20:58651931-58652145 | Rare:65; Clinvar (benign):2 | ||||
| chr20:58652345-58652619 | Common:2; Rare:89 | ||||
| chr20:58888768-58888991 | Common:1; Rare:66 | ||||
| chr20:58910331-58910629 | Common:2; Rare:64 | ||||
| chr20:58981163-58981316 | Common:2; Rare:80 | ||||
| chr20:58990792-58990982 | Common:1; Rare:50 | ||||
| chr20:58991029-58991311 | Common:1; Rare:63 | ||||
| chr20:59032218-59032568 | Common:3; Rare:149; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:59042712-59043022 | Common:1; Rare:114 | ||||
| chr20:59933594-59933798 | Common:4; Rare:82 | ||||
| chr20:59940285-59940481 | Rare:82 | ||||
| chr20:62139082-62139291 | Common:1; Rare:64 | ||||
| chr20:62143230-62143835 | Common:8; Rare:245 | ||||
| chr20:62182942-62183050 | Rare:30 |