| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29145373-29145630 | Rare:48 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732036-31732341 | Common:5; Rare:146 | ||||
| chr21:32278999-32279205 | Common:3; Rare:93 | ||||
| chr21:32392945-32393187 | Common:3; Rare:105 | ||||
| chr21:32612522-32612900 | Rare:95 | ||||
| chr21:32771718-32772161 | Common:13; Rare:196 | ||||
| chr21:33025584-33025935 | Common:1; Rare:87 | ||||
| chr21:33266241-33266430 | Rare:54; Clinvar:3 | ||||
| chr21:33324862-33325068 | Common:4; Rare:85 | ||||
| chr21:33479859-33480201 | Common:1; Rare:110 | ||||
| chr21:33542070-33542279 | Rare:85 | ||||
| chr21:33542805-33543121 | Common:3; Rare:118 | ||||
| chr21:34526795-34527171 | Common:1; Rare:68 | ||||
| chr21:35049267-35049451 | Common:1; Rare:28 |