| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31731955-31732398 | Common:5; Rare:193 | ||||
| chr21:32279010-32279214 | Common:3; Rare:86 | ||||
| chr21:32392906-32393171 | Common:2; Rare:111 | ||||
| chr21:32411597-32411811 | Rare:52 | ||||
| chr21:32412605-32412853 | Rare:61 | ||||
| chr21:32727850-32728171 | Rare:145; Clinvar:2 | ||||
| chr21:32771702-32772246 | Common:14; Rare:230 | ||||
| chr21:32813670-32813905 | Rare:51 | ||||
| chr21:33266262-33266528 | Rare:80; Clinvar:3 | ||||
| chr21:33324847-33325097 | Common:4; Rare:109 | ||||
| chr21:33479837-33480204 | Common:1; Rare:116 | ||||
| chr21:33542077-33542191 | Rare:40 | ||||
| chr21:33542814-33543357 | Common:2; Rare:200 | ||||
| chr21:33566895-33567188 | Common:3; Rare:58 |