| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34302899-34303162 | Rare:85 | ||||
| chr20:34303251-34303569 | Common:2; Rare:118; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:34363137-34363377 | Rare:66 | ||||
| chr20:34515817-34515980 | Rare:30 | ||||
| chr20:34516263-34516530 | Common:4; Rare:110 | ||||
| chr20:34516595-34516776 | Rare:67 | ||||
| chr20:34516804-34516916 | Rare:37 | ||||
| chr20:34558518-34558758 | Common:1; Rare:65 | ||||
| chr20:34676511-34676917 | Common:1; Rare:99 | ||||
| chr20:34676999-34677420 | Rare:108 | ||||
| chr20:34677528-34677562 | Rare:12 | ||||
| chr20:34704093-34704384 | Common:1; Rare:90 | ||||
| chr20:34704572-34704767 | Common:2; Rare:42 | ||||
| chr20:34825230-34825419 | Common:1; Rare:50 | ||||
| chr20:34825648-34825848 | Rare:89 |