| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29024526-29024726 | Common:2; Rare:86 | ||||
| chr21:29073597-29073860 | Common:2; Rare:76 | ||||
| chr21:29298594-29298953 | Common:3; Rare:138 | ||||
| chr21:31659515-31659791 | Common:2; Rare:124; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr21:32279012-32279214 | Common:3; Rare:86 | ||||
| chr21:32392957-32393179 | Common:2; Rare:94 | ||||
| chr21:32612557-32612884 | Rare:80 | ||||
| chr21:32727897-32728125 | Rare:111; Clinvar:2 | ||||
| chr21:32771724-32772163 | Common:13; Rare:196 | ||||
| chr21:33266284-33266473 | Rare:62; Clinvar:3 | ||||
| chr21:33324866-33325039 | Common:4; Rare:73 | ||||
| chr21:33479816-33480204 | Common:1; Rare:120 | ||||
| chr21:33542080-33542248 | Rare:67 | ||||
| chr21:33542805-33543136 | Common:3; Rare:120 | ||||
| chr21:34526763-34527077 | Common:1; Rare:61 |