| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33401483-33401584 | Rare:28 | ||||
| chr20:33993759-33994128 | Common:2; Rare:132 | ||||
| chr20:34112096-34112417 | Rare:104 | ||||
| chr20:34302988-34303337 | Common:1; Rare:132; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:34516264-34516451 | Common:3; Rare:75 | ||||
| chr20:34558533-34558776 | Common:1; Rare:63 | ||||
| chr20:34677086-34677294 | Rare:54 | ||||
| chr20:34955733-34955868 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:35092618-35092938 | Common:2; Rare:140 | ||||
| chr20:35147265-35147411 | Common:1; Rare:54 | ||||
| chr20:35171963-35172146 | Rare:40 | ||||
| chr20:35278034-35278281 | Common:7; Rare:86 | ||||
| chr20:35284552-35284870 | Common:2; Rare:85 | ||||
| chr20:35455066-35455201 | Common:1; Rare:48 | ||||
| chr20:35664867-35665004 | Common:1; Rare:38 |