| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44210718-44211105 | Common:5; Rare:141 | ||||
| chr20:44475780-44475935 | Rare:68 | ||||
| chr20:44522001-44522206 | Common:2; Rare:64 | ||||
| chr20:44531820-44531978 | Common:1; Rare:50 | ||||
| chr20:44651687-44651789 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr20:44885382-44885794 | Common:8; Rare:135 | ||||
| chr20:44909943-44910137 | Common:2; Rare:87 | ||||
| chr20:44960366-44960509 | Common:1; Rare:55 | ||||
| chr20:44966316-44966566 | Common:1; Rare:100 | ||||
| chr20:45363353-45363521 | Common:1; Rare:41 | ||||
| chr20:45416017-45416159 | Rare:40 | ||||
| chr20:45791912-45791987 | Rare:26 | ||||
| chr20:45812311-45812698 | Common:4; Rare:112 | ||||
| chr20:45812836-45813044 | Common:2; Rare:40 | ||||
| chr20:45857320-45857634 | Common:3; Rare:89 |