| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47501746-47501993 | Common:1; Rare:86 | ||||
| chr20:48921615-48921783 | Common:1; Rare:68 | ||||
| chr20:49046183-49046341 | Common:2; Rare:43 | ||||
| chr20:49219197-49219464 | Common:1; Rare:120 | ||||
| chr20:49278038-49278239 | Rare:55 | ||||
| chr20:49278436-49278698 | Common:8; Rare:101 | ||||
| chr20:49915461-49915602 | Common:3; Rare:55 | ||||
| chr20:50113127-50113343 | Common:6; Rare:78 | ||||
| chr20:50153633-50153962 | Common:2; Rare:133 | ||||
| chr20:50958499-50958840 | Common:1; Rare:108; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:52191687-52191943 | Common:1; Rare:61 | ||||
| chr20:56392213-56392704 | Common:6; Rare:130 | ||||
| chr20:56468431-56468718 | Rare:100 | ||||
| chr20:58309427-58309715 | Common:2; Rare:114 | ||||
| chr20:58651131-58651399 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):1 |