| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:32207676-32207953 | Common:3; Rare:107 | ||||
| chr20:33401458-33401625 | Rare:46 | ||||
| chr20:33811172-33811499 | Common:1; Rare:102 | ||||
| chr20:33993078-33993285 | Rare:55 | ||||
| chr20:33994069-33994122 | Rare:15 | ||||
| chr20:34112102-34112430 | Rare:109 | ||||
| chr20:34516333-34516451 | Rare:49 | ||||
| chr20:34558550-34558776 | Common:1; Rare:60 | ||||
| chr20:34677086-34677290 | Rare:53 | ||||
| chr20:34955741-34955836 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:35147247-35147416 | Common:1; Rare:60 | ||||
| chr20:35172039-35172167 | Rare:36 | ||||
| chr20:35278023-35278333 | Common:7; Rare:104 | ||||
| chr20:35284545-35284623 | Common:1; Rare:9 | ||||
| chr20:35284728-35284863 | Common:1; Rare:46 |