| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29024876-29025025 | Rare:29 | ||||
| chr21:29073578-29073870 | Common:2; Rare:88 | ||||
| chr21:29194003-29194166 | Common:2; Rare:29 | ||||
| chr21:29298600-29298935 | Common:2; Rare:129 | ||||
| chr21:31659493-31659838 | Common:2; Rare:154; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732062-31732332 | Common:5; Rare:125 | ||||
| chr21:32279010-32279205 | Common:3; Rare:85 | ||||
| chr21:32392906-32393197 | Common:4; Rare:123 | ||||
| chr21:32411636-32411786 | Rare:36 | ||||
| chr21:32412168-32412519 | Common:2; Rare:76 | ||||
| chr21:32412776-32412870 | Rare:26 | ||||
| chr21:32612483-32612947 | Rare:123 | ||||
| chr21:32727875-32728129 | Rare:121; Clinvar:2 | ||||
| chr21:32771715-32772237 | Common:14; Rare:223 | ||||
| chr21:33266294-33266458 | Rare:55; Clinvar:3 |