| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44210710-44211105 | Common:5; Rare:143 | ||||
| chr20:44311149-44311312 | Common:1; Rare:58 | ||||
| chr20:44475772-44475905 | Rare:56 | ||||
| chr20:44522015-44522180 | Common:2; Rare:56 | ||||
| chr20:44651662-44651831 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr20:44885426-44885827 | Common:7; Rare:122 | ||||
| chr20:44909887-44910140 | Common:2; Rare:106 | ||||
| chr20:44960334-44960514 | Common:1; Rare:76 | ||||
| chr20:44966370-44966568 | Common:1; Rare:78 | ||||
| chr20:45362941-45363232 | Rare:89 | ||||
| chr20:45363340-45363527 | Common:1; Rare:44 | ||||
| chr20:45406541-45406759 | Rare:57 | ||||
| chr20:45407067-45407307 | Common:1; Rare:36 | ||||
| chr20:45416005-45416194 | Rare:68; Clinvar:1 | ||||
| chr20:45791898-45792047 | Common:3; Rare:63 |