| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44521986-44522228 | Common:2; Rare:76 | ||||
| chr20:44531961-44531985 | Common:1; Rare:2 | ||||
| chr20:44715152-44715402 | Common:29; Rare:79 | ||||
| chr20:44885602-44885883 | Common:4; Rare:93 | ||||
| chr20:44960366-44960686 | Common:2; Rare:87 | ||||
| chr20:44966370-44966566 | Rare:78 | ||||
| chr20:45348418-45348593 | Common:1; Rare:48 | ||||
| chr20:45363346-45363528 | Common:1; Rare:44 | ||||
| chr20:45406325-45406726 | Common:1; Rare:105 | ||||
| chr20:45415959-45416159 | Rare:53 | ||||
| chr20:45416302-45416625 | Rare:98; Clinvar (pathogenic):2 | ||||
| chr20:45420356-45420635 | Rare:96; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr20:45791904-45791996 | Rare:36 | ||||
| chr20:45833756-45833940 | Common:7; Rare:42 | ||||
| chr20:45857342-45857633 | Common:3; Rare:76 |