| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63981035-63981230 | Common:4; Rare:65; Clinvar:7; Clinvar (benign):4 | ||||
| chr21:14383115-14383469 | Common:2; Rare:99 | ||||
| chr21:25734853-25735463 | Common:4; Rare:215 | ||||
| chr21:25735531-25735721 | Rare:52 | ||||
| chr21:26845397-26845555 | Common:1; Rare:39 | ||||
| chr21:28885312-28885425 | Common:3; Rare:84 | ||||
| chr21:28992818-28993113 | Common:2; Rare:125 | ||||
| chr21:29019297-29019395 | Common:5; Rare:45 | ||||
| chr21:29024520-29024738 | Common:2; Rare:93 | ||||
| chr21:29073592-29073857 | Common:2; Rare:79 | ||||
| chr21:29298771-29298942 | Common:1; Rare:74 | ||||
| chr21:31659502-31659806 | Common:2; Rare:138; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr21:32392956-32393197 | Common:4; Rare:103 | ||||
| chr21:32612319-32612866 | Rare:134 | ||||
| chr21:32727901-32728122 | Rare:106; Clinvar:2 |