| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44210701-44211115 | Common:5; Rare:149 | ||||
| chr20:44355577-44355738 | Common:1; Rare:24; Clinvar:1 | ||||
| chr20:44475791-44475954 | Common:1; Rare:69 | ||||
| chr20:44521980-44522260 | Common:3; Rare:84 | ||||
| chr20:44582541-44582608 | Rare:10 | ||||
| chr20:44651688-44651810 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chr20:44960370-44960522 | Common:1; Rare:55 | ||||
| chr20:44966376-44966574 | Common:1; Rare:77 | ||||
| chr20:45348332-45348593 | Common:2; Rare:82 | ||||
| chr20:45362956-45363315 | Rare:106 | ||||
| chr20:45363353-45363487 | Rare:27 | ||||
| chr20:45416044-45416621 | Rare:197; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr20:45791913-45791996 | Rare:33 | ||||
| chr20:45857308-45857621 | Common:4; Rare:86 | ||||
| chr20:45891165-45891413 | Common:1; Rare:77; Clinvar:3; Clinvar (benign):1 |