| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44521914-44522224 | Common:4; Rare:175 | ||||
| chr20:44531771-44532370 | Common:8; Rare:261 | ||||
| chr20:44651686-44651845 | Common:1; Rare:70; Clinvar (benign):1 | ||||
| chr20:44885382-44885785 | Common:14; Rare:242 | ||||
| chr20:44921410-44921850 | Common:1; Rare:113 | ||||
| chr20:44960325-44960521 | Common:2; Rare:156 | ||||
| chr20:44966313-44966571 | Common:4; Rare:185 | ||||
| chr20:45362929-45363208 | Rare:84 | ||||
| chr20:45363332-45363505 | Common:1; Rare:36 | ||||
| chr20:45363427-45363532 | Common:1; Rare:29 | ||||
| chr20:45406538-45406717 | Rare:79 | ||||
| chr20:45415999-45416174 | Rare:95 | ||||
| chr20:45416385-45416629 | Rare:66; Clinvar (pathogenic):2 | ||||
| chr20:45791851-45792095 | Common:4; Rare:138 | ||||
| chr20:45833135-45833650 | Common:14; Rare:141 |