| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:32429767-32430115 | Common:2; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:32483440-32483666 | Rare:45 | ||||
| chr20:32743311-32743619 | Common:1; Rare:72 | ||||
| chr20:33401504-33401625 | Rare:31 | ||||
| chr20:33489832-33490166 | Common:2; Rare:114 | ||||
| chr20:33993063-33993291 | Rare:62 | ||||
| chr20:33993500-33994128 | Common:3; Rare:199 | ||||
| chr20:34076767-34077240 | Common:8; Rare:197 | ||||
| chr20:34112204-34112427 | Rare:66 | ||||
| chr20:34516327-34516455 | Common:1; Rare:53 | ||||
| chr20:34558560-34558907 | Common:1; Rare:102 | ||||
| chr20:34677033-34677131 | Rare:39 | ||||
| chr20:34872805-34872896 | Rare:34 | ||||
| chr20:34955689-34955929 | Common:1; Rare:88; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:35147301-35147406 | Rare:29 |