| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:7302538-7302688 | Rare:27 | ||||
| chr20:9067668-9067938 | Common:3; Rare:61 | ||||
| chr20:9573229-9573771 | Common:6; Rare:181 | ||||
| chr20:9574120-9574530 | Common:2; Rare:85 | ||||
| chr20:10119350-10119650 | Common:2; Rare:49 | ||||
| chr20:10217918-10218318 | Common:2; Rare:130 | ||||
| chr20:10466340-10466780 | Common:4; Rare:70 | ||||
| chr20:10490770-10491130 | Common:7; Rare:59 | ||||
| chr20:10540597-10540997 | Rare:98 | ||||
| chr20:10604450-10604760 | Common:1; Rare:60 | ||||
| chr20:10629936-10630265 | Common:2; Rare:60 | ||||
| chr20:10630312-10630712 | Common:4; Rare:152 | ||||
| chr20:10637499-10637936 | Common:1; Rare:139; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:10655780-10656110 | Rare:60 | ||||
| chr20:10674662-10675062 | Common:6; Rare:112 |