| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31605102-31605811 | Common:12; Rare:380 | ||||
| chr20:31722791-31722942 | Rare:40 | ||||
| chr20:31723523-31723768 | Common:1; Rare:81 | ||||
| chr20:31739109-31739357 | Common:1; Rare:62 | ||||
| chr20:32207658-32208027 | Common:4; Rare:132 | ||||
| chr20:32483360-32483702 | Rare:59 | ||||
| chr20:33401481-33401589 | Rare:29 | ||||
| chr20:33666672-33666981 | Rare:79 | ||||
| chr20:33993078-33993291 | Rare:57 | ||||
| chr20:34073495-34073655 | Rare:28 | ||||
| chr20:34516327-34516451 | Common:1; Rare:50 | ||||
| chr20:34677063-34677329 | Rare:74 | ||||
| chr20:34874888-34875102 | Common:2; Rare:48 | ||||
| chr20:34882543-34882808 | Common:1; Rare:49 | ||||
| chr20:34955725-34955832 | Common:1; Rare:41; Clinvar:3; Clinvar (benign):3 |