| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44885285-44885324 | Rare:13 | ||||
| chr20:44885366-44885795 | Common:8; Rare:138 | ||||
| chr20:44886021-44886084 | Rare:21 | ||||
| chr20:44886135-44886147 | Rare:3 | ||||
| chr20:44909882-44910174 | Common:2; Rare:122 | ||||
| chr20:44960258-44960594 | Common:1; Rare:123 | ||||
| chr20:44966202-44966599 | Common:2; Rare:135 | ||||
| chr20:45348379-45348555 | Common:1; Rare:51 | ||||
| chr20:45362909-45363270 | Common:1; Rare:108 | ||||
| chr20:45363328-45363550 | Common:2; Rare:56 | ||||
| chr20:45406513-45406763 | Rare:68 | ||||
| chr20:45415919-45416231 | Rare:102; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr20:45416364-45416478 | Rare:28 | ||||
| chr20:45469427-45469755 | Common:1; Rare:80 | ||||
| chr20:45470436-45470839 | Common:1; Rare:118 |