| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26845405-26845609 | Common:2; Rare:54 | ||||
| chr21:28885337-28885410 | Common:2; Rare:57 | ||||
| chr21:28992781-28993120 | Common:2; Rare:139 | ||||
| chr21:29019312-29019443 | Common:5; Rare:54 | ||||
| chr21:29024537-29024738 | Common:2; Rare:91 | ||||
| chr21:29024876-29025019 | Rare:28 | ||||
| chr21:29073592-29073870 | Common:2; Rare:83 | ||||
| chr21:30480359-30480443 | Rare:14 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732062-31732319 | Common:5; Rare:119 | ||||
| chr21:32278955-32279212 | Common:3; Rare:119 | ||||
| chr21:32335882-32336278 | Common:1; Rare:79 | ||||
| chr21:32392956-32393187 | Common:3; Rare:99 | ||||
| chr21:32603195-32603376 | Common:1; Rare:63; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr21:32612170-32612910 | Common:3; Rare:196; Clinvar:2 |