| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50113125-50113261 | Common:5; Rare:64 | ||||
| chr20:50115941-50116074 | Common:1; Rare:30 | ||||
| chr20:50153588-50153914 | Common:3; Rare:123 | ||||
| chr20:50510135-50510434 | Common:3; Rare:116 | ||||
| chr20:50794854-50795099 | Common:1; Rare:90 | ||||
| chr20:50958481-50958850 | Common:1; Rare:129; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:56392153-56392401 | Rare:70 | ||||
| chr20:56392404-56392687 | Common:6; Rare:70 | ||||
| chr20:56468431-56468700 | Rare:97 | ||||
| chr20:57266076-57266334 | Common:1; Rare:65 | ||||
| chr20:57266634-57266759 | Rare:41 | ||||
| chr20:57351178-57351285 | Common:2; Rare:29 | ||||
| chr20:58388984-58389277 | Common:3; Rare:132; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:58651091-58651305 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58888788-58888841 | Rare:19 |