| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:25734851-25735485 | Common:5; Rare:218 | ||||
| chr21:25735510-25735715 | Rare:56 | ||||
| chr21:26170562-26170895 | Common:3; Rare:110; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:26845379-26845555 | Common:1; Rare:42 | ||||
| chr21:28992773-28993067 | Common:1; Rare:127 | ||||
| chr21:29019297-29019386 | Common:5; Rare:43 | ||||
| chr21:29024537-29024768 | Common:2; Rare:102 | ||||
| chr21:29024876-29024997 | Rare:22 | ||||
| chr21:29073586-29073860 | Common:2; Rare:81 | ||||
| chr21:30216022-30216286 | Common:1; Rare:50 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:32279010-32279157 | Common:1; Rare:66 | ||||
| chr21:32392906-32393209 | Common:4; Rare:126 | ||||
| chr21:32411600-32411811 | Rare:50 | ||||
| chr21:32612483-32612874 | Rare:100 |