| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29024876-29024979 | Rare:19 | ||||
| chr21:29073592-29073727 | Common:2; Rare:47 | ||||
| chr21:29298749-29298956 | Common:2; Rare:90 | ||||
| chr21:29299091-29299420 | Common:1; Rare:106 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:32279017-32279219 | Common:3; Rare:85 | ||||
| chr21:32392956-32393179 | Common:2; Rare:94 | ||||
| chr21:32612544-32612872 | Rare:80 | ||||
| chr21:32727889-32728122 | Rare:113; Clinvar:2 | ||||
| chr21:32771707-32772167 | Common:13; Rare:203 | ||||
| chr21:33266262-33266466 | Rare:66; Clinvar:3 | ||||
| chr21:33324854-33325065 | Common:4; Rare:88 | ||||
| chr21:33479822-33480147 | Rare:108 | ||||
| chr21:33542080-33542248 | Rare:67 | ||||
| chr21:33542803-33543168 | Common:3; Rare:122 |