| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:38962145-38962388 | Common:1; Rare:101 | ||||
| chr20:40688741-40688861 | Rare:33 | ||||
| chr20:40689232-40689538 | Common:2; Rare:93 | ||||
| chr20:41028528-41028903 | Rare:136 | ||||
| chr20:41340614-41340987 | Common:1; Rare:87 | ||||
| chr20:43458256-43458504 | Common:3; Rare:90 | ||||
| chr20:43590650-43590996 | Rare:78 | ||||
| chr20:44187473-44187737 | Common:1; Rare:47 | ||||
| chr20:44210524-44211117 | Common:6; Rare:204 | ||||
| chr20:44475819-44475964 | Common:1; Rare:56 | ||||
| chr20:44651687-44651807 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chr20:44714548-44714961 | Rare:92 | ||||
| chr20:44960345-44960521 | Common:1; Rare:72 | ||||
| chr20:44966316-44966566 | Common:1; Rare:100 | ||||
| chr20:45363383-45363558 | Common:2; Rare:52 |