| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:26842747-26843041 | Common:5; Rare:56 | ||||
| chr21:26845345-26845555 | Common:1; Rare:55 | ||||
| chr21:29019312-29019395 | Common:5; Rare:37 | ||||
| chr21:29024537-29024726 | Common:2; Rare:84 | ||||
| chr21:29024876-29025012 | Rare:25 | ||||
| chr21:29073592-29073854 | Common:2; Rare:78 | ||||
| chr21:29298737-29298935 | Common:1; Rare:84 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:32278990-32279164 | Common:2; Rare:82 | ||||
| chr21:32392956-32393179 | Common:2; Rare:94 | ||||
| chr21:32411631-32411802 | Rare:41 | ||||
| chr21:32412379-32412737 | Common:2; Rare:76 | ||||
| chr21:32727896-32728129 | Rare:115; Clinvar:2 | ||||
| chr21:32771702-32772167 | Common:13; Rare:205 | ||||
| chr21:33266262-33266443 | Rare:58; Clinvar:3 |