| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:37289578-37289674 | Common:1; Rare:30 | ||||
| chr20:38033417-38033818 | Common:2; Rare:120 | ||||
| chr20:44187446-44187771 | Common:1; Rare:56 | ||||
| chr20:44210705-44211105 | Common:5; Rare:144 | ||||
| chr20:44651658-44651848 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr20:44966320-44966568 | Common:2; Rare:100 | ||||
| chr20:45791912-45791972 | Rare:21 | ||||
| chr20:45857326-45857621 | Common:3; Rare:79 | ||||
| chr20:45891258-45891435 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45910901-45911163 | Common:4; Rare:73 | ||||
| chr20:46364364-46364538 | Rare:66 | ||||
| chr20:46406575-46406787 | Common:1; Rare:56 | ||||
| chr20:47318993-47319123 | Common:1; Rare:36 | ||||
| chr20:48921498-48921770 | Common:2; Rare:98 | ||||
| chr20:49219261-49219469 | Common:1; Rare:100 |