| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43789369-43789624 | Common:1; Rare:93 | ||||
| chr21:44299974-44300114 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr21:44801763-44801858 | Rare:44 | ||||
| chr21:44873618-44874070 | Common:9; Rare:178 | ||||
| chr21:44910701-44911065 | Common:4; Rare:88; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr21:44939874-44940060 | Common:2; Rare:53 | ||||
| chr21:45287864-45288087 | Common:6; Rare:89 | ||||
| chr21:45981519-45981773 | Common:23; Rare:49; Clinvar (benign):1 | ||||
| chr21:46184404-46184745 | Common:4; Rare:32 | ||||
| chr21:46286025-46286396 | Common:5; Rare:118 | ||||
| chr21:46323790-46324153 | Common:2; Rare:130; Clinvar (benign):1 | ||||
| chr21:46324459-46324686 | Common:4; Rare:83 | ||||
| chr21:46458686-46459059 | Common:3; Rare:128 | ||||
| chr21:46635457-46635737 | Common:6; Rare:95 | ||||
| chr22:17159183-17159376 | Common:5; Rare:86 |