| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29019215-29019433 | Common:5; Rare:84 | ||||
| chr21:29024518-29024773 | Common:2; Rare:105 | ||||
| chr21:29061615-29061737 | Common:1; Rare:21 | ||||
| chr21:29062123-29062555 | Common:1; Rare:101 | ||||
| chr21:29073501-29073850 | Common:2; Rare:107 | ||||
| chr21:29298617-29298953 | Common:3; Rare:133 | ||||
| chr21:31659491-31659858 | Common:2; Rare:163; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31731951-31732271 | Common:4; Rare:133 | ||||
| chr21:32278985-32279214 | Common:3; Rare:102 | ||||
| chr21:32392845-32393172 | Common:2; Rare:131 | ||||
| chr21:32412701-32412763 | Rare:14 | ||||
| chr21:32612087-32612195 | Rare:31; Clinvar:3; Clinvar (benign):1 | ||||
| chr21:32727893-32728139 | Rare:120; Clinvar:2 | ||||
| chr21:32771333-32771397 | Rare:29 | ||||
| chr21:32771637-32772057 | Common:13; Rare:192 |