| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50113107-50113223 | Common:5; Rare:57 | ||||
| chr20:50153647-50153881 | Common:2; Rare:94 | ||||
| chr20:50958478-50958867 | Common:1; Rare:145; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:52972562-52972775 | Common:2; Rare:43 | ||||
| chr20:56392187-56392692 | Common:6; Rare:133 | ||||
| chr20:57329653-57329851 | Common:1; Rare:90 | ||||
| chr20:57709997-57710385 | Common:2; Rare:107 | ||||
| chr20:57711392-57711445 | Rare:10 | ||||
| chr20:57711457-57711484 | Rare:7 | ||||
| chr20:58150839-58150958 | Rare:46 | ||||
| chr20:58651135-58651305 | Common:2; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58888788-58888820 | Rare:9 | ||||
| chr20:58888826-58888866 | Rare:12 | ||||
| chr20:59032240-59032551 | Common:3; Rare:130; Clinvar (benign):5 | ||||
| chr20:59042763-59043063 | Common:1; Rare:112 |