| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29024526-29024747 | Common:2; Rare:98 | ||||
| chr21:29024876-29025053 | Rare:34 | ||||
| chr21:29073586-29073856 | Common:2; Rare:81 | ||||
| chr21:29298549-29298965 | Common:3; Rare:155 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732056-31732300 | Common:4; Rare:107 | ||||
| chr21:32279011-32279219 | Common:3; Rare:87 | ||||
| chr21:32392956-32393187 | Common:3; Rare:99 | ||||
| chr21:32411591-32411822 | Rare:56 | ||||
| chr21:32612507-32612903 | Rare:100 | ||||
| chr21:32727896-32728129 | Rare:115; Clinvar:2 | ||||
| chr21:32771715-32772246 | Common:14; Rare:224 | ||||
| chr21:33266262-33266458 | Rare:64; Clinvar:3 | ||||
| chr21:33324862-33325065 | Common:4; Rare:85 | ||||
| chr21:33479843-33480173 | Common:1; Rare:111 |