| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26844836-26844956 | Common:1; Rare:41 | ||||
| chr21:26845042-26845251 | Common:2; Rare:40 | ||||
| chr21:26845285-26845604 | Common:2; Rare:91 | ||||
| chr21:28992781-28993159 | Common:2; Rare:151 | ||||
| chr21:29019321-29019407 | Common:5; Rare:32 | ||||
| chr21:29024534-29024726 | Common:2; Rare:85 | ||||
| chr21:29073592-29073854 | Common:2; Rare:78 | ||||
| chr21:29298649-29298942 | Common:2; Rare:118 | ||||
| chr21:31659502-31659835 | Common:2; Rare:149; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:32392906-32393171 | Common:2; Rare:111 | ||||
| chr21:32411600-32411822 | Rare:53 | ||||
| chr21:32412228-32412543 | Common:3; Rare:71 | ||||
| chr21:32612230-32612620 | Common:3; Rare:108 | ||||
| chr21:32727897-32728167 | Rare:130; Clinvar:2 | ||||
| chr21:32771724-32772161 | Common:13; Rare:195 |