| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33993771-33994130 | Common:1; Rare:128 | ||||
| chr20:34112089-34112425 | Rare:106 | ||||
| chr20:34302965-34303361 | Common:1; Rare:154; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:34516265-34516451 | Common:3; Rare:75 | ||||
| chr20:34558507-34558789 | Common:1; Rare:75 | ||||
| chr20:34559103-34559229 | Rare:44 | ||||
| chr20:34677063-34677299 | Rare:66 | ||||
| chr20:34825496-34825819 | Rare:126 | ||||
| chr20:34872811-34872927 | Rare:42 | ||||
| chr20:34876288-34876665 | Common:3; Rare:103 | ||||
| chr20:34955724-34955929 | Common:1; Rare:79; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:35147265-35147461 | Common:1; Rare:68 | ||||
| chr20:35171846-35171979 | Rare:24 | ||||
| chr20:35171997-35172184 | Rare:47 | ||||
| chr20:35284544-35284880 | Common:2; Rare:90 |