| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49915481-49915560 | Common:2; Rare:31 | ||||
| chr20:50113106-50113244 | Common:5; Rare:69 | ||||
| chr20:50909833-50909969 | Common:1; Rare:28 | ||||
| chr20:50931401-50931696 | Common:2; Rare:110 | ||||
| chr20:50958478-50958923 | Common:1; Rare:167; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:53593781-53593914 | Common:1; Rare:50 | ||||
| chr20:54207938-54208110 | Rare:42 | ||||
| chr20:56392197-56392687 | Common:6; Rare:127 | ||||
| chr20:56630027-56630232 | Rare:51 | ||||
| chr20:58309421-58309715 | Common:2; Rare:115 | ||||
| chr20:58515317-58515528 | Common:3; Rare:43 | ||||
| chr20:58651095-58651771 | Common:3; Rare:161; Clinvar:4; Clinvar (benign):6 | ||||
| chr20:58888777-58888820 | Rare:14 | ||||
| chr20:58990728-58991033 | Common:1; Rare:74 | ||||
| chr20:58991215-58991422 | Common:1; Rare:59 |