| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44311149-44311314 | Common:1; Rare:58 | ||||
| chr20:44475813-44475938 | Rare:50 | ||||
| chr20:44522002-44522231 | Common:2; Rare:71 | ||||
| chr20:44531794-44531978 | Common:1; Rare:58 | ||||
| chr20:44651687-44651831 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr20:44885407-44885850 | Common:7; Rare:132 | ||||
| chr20:44960345-44960521 | Common:1; Rare:72 | ||||
| chr20:44966314-44966588 | Common:2; Rare:106 | ||||
| chr20:45348404-45348575 | Common:1; Rare:44 | ||||
| chr20:45363108-45363251 | Rare:45 | ||||
| chr20:45363306-45363556 | Common:2; Rare:67 | ||||
| chr20:45416005-45416334 | Rare:123; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr20:45791912-45792036 | Common:2; Rare:51 | ||||
| chr20:45812330-45812698 | Common:4; Rare:107 | ||||
| chr20:45833717-45833838 | Common:2; Rare:30 |