| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33401481-33401634 | Rare:41 | ||||
| chr20:33666367-33666524 | Rare:39 | ||||
| chr20:33666674-33666718 | Rare:9 | ||||
| chr20:33993064-33993271 | Rare:57 | ||||
| chr20:33993672-33993993 | Common:3; Rare:108 | ||||
| chr20:33994009-33994130 | Rare:37 | ||||
| chr20:34112094-34112384 | Rare:89 | ||||
| chr20:34516265-34516451 | Common:3; Rare:75 | ||||
| chr20:34558518-34558767 | Common:1; Rare:70 | ||||
| chr20:34677081-34677298 | Rare:57 | ||||
| chr20:34872691-34872899 | Rare:59 | ||||
| chr20:34955725-34955928 | Common:1; Rare:77; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:35092651-35092938 | Common:2; Rare:125 | ||||
| chr20:35171657-35172020 | Common:2; Rare:63 | ||||
| chr20:35172039-35172177 | Rare:39 |