| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44210710-44211117 | Common:5; Rare:149 | ||||
| chr20:44475759-44475923 | Rare:77 | ||||
| chr20:44522028-44522215 | Common:2; Rare:58 | ||||
| chr20:44885371-44885817 | Common:8; Rare:144 | ||||
| chr20:44909935-44910096 | Common:2; Rare:59 | ||||
| chr20:44960341-44960686 | Common:2; Rare:103 | ||||
| chr20:44966406-44966586 | Common:1; Rare:64 | ||||
| chr20:45406147-45406178 | Rare:8 | ||||
| chr20:45406541-45406714 | Rare:44 | ||||
| chr20:45791916-45792034 | Common:2; Rare:47 | ||||
| chr20:45812330-45812703 | Common:4; Rare:107 | ||||
| chr20:45834076-45834183 | Rare:39 | ||||
| chr20:45857342-45857633 | Common:3; Rare:76 | ||||
| chr20:45881072-45881241 | Common:2; Rare:38 | ||||
| chr20:45891250-45891387 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 |