| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49278020-49278272 | Rare:67 | ||||
| chr20:49568045-49568152 | Common:1; Rare:27 | ||||
| chr20:49812573-49812926 | Common:3; Rare:81 | ||||
| chr20:49915471-49915585 | Common:3; Rare:41 | ||||
| chr20:50113106-50113244 | Common:5; Rare:69 | ||||
| chr20:50115935-50116080 | Common:1; Rare:34 | ||||
| chr20:50691334-50691638 | Rare:55 | ||||
| chr20:50930355-50930640 | Common:3; Rare:100 | ||||
| chr20:50958487-50958851 | Common:1; Rare:126; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:56392001-56392704 | Common:8; Rare:188 | ||||
| chr20:56468312-56468710 | Rare:127 | ||||
| chr20:57266126-57266406 | Common:1; Rare:70 | ||||
| chr20:57710013-57710283 | Common:1; Rare:79 | ||||
| chr20:57710547-57710668 | Rare:33 | ||||
| chr20:58388984-58389297 | Common:3; Rare:146; Clinvar:4; Clinvar (benign):1 |