| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33401473-33401653 | Rare:52 | ||||
| chr20:33562178-33562588 | Rare:66 | ||||
| chr20:33720205-33720585 | Common:4; Rare:93 | ||||
| chr20:33731987-33732012 | Rare:13 | ||||
| chr20:33993048-33993268 | Common:1; Rare:58 | ||||
| chr20:33993759-33994125 | Common:2; Rare:131 | ||||
| chr20:34112094-34112441 | Rare:113 | ||||
| chr20:34302958-34303153 | Rare:63 | ||||
| chr20:34303286-34303492 | Common:2; Rare:90; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:34363171-34363331 | Rare:41 | ||||
| chr20:34516326-34516455 | Common:1; Rare:54 | ||||
| chr20:34676515-34676864 | Common:1; Rare:80 | ||||
| chr20:34677063-34677350 | Rare:78 | ||||
| chr20:34825511-34825819 | Rare:121 | ||||
| chr20:34872811-34872932 | Rare:43 |