| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31547294-31547437 | Rare:35 | ||||
| chr20:31722731-31722886 | Rare:35 | ||||
| chr20:31722893-31723034 | Rare:30 | ||||
| chr20:31845542-31845753 | Common:1; Rare:45 | ||||
| chr20:32207676-32207939 | Common:3; Rare:97 | ||||
| chr20:33401481-33401625 | Rare:38 | ||||
| chr20:33731979-33732005 | Rare:14 | ||||
| chr20:34112096-34112423 | Rare:104 | ||||
| chr20:34516307-34516451 | Common:3; Rare:56 | ||||
| chr20:34677084-34677294 | Rare:55 | ||||
| chr20:34955725-34955896 | Common:1; Rare:69; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:35092658-35092956 | Common:2; Rare:122 | ||||
| chr20:35147229-35147428 | Common:1; Rare:70 | ||||
| chr20:35171705-35172114 | Common:2; Rare:78 | ||||
| chr20:35556715-35557004 | Common:2; Rare:74 |