| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43659443-43659614 | Common:1; Rare:56 | ||||
| chr21:43789375-43789638 | Common:1; Rare:99 | ||||
| chr21:44339209-44339457 | Common:2; Rare:76 | ||||
| chr21:44801766-44801880 | Rare:49 | ||||
| chr21:44873672-44874050 | Common:7; Rare:153 | ||||
| chr21:44939871-44940031 | Common:2; Rare:43 | ||||
| chr21:45287879-45288112 | Common:5; Rare:88 | ||||
| chr21:45981500-45981841 | Common:23; Rare:85; Clinvar (benign):2 | ||||
| chr21:46184429-46184764 | Common:4; Rare:28 | ||||
| chr21:46286260-46286407 | Common:4; Rare:53 | ||||
| chr21:46286541-46286665 | Common:1; Rare:33 | ||||
| chr21:46323830-46324222 | Common:3; Rare:143; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46635502-46635737 | Common:5; Rare:77 | ||||
| chr22:17159207-17159393 | Common:4; Rare:96 | ||||
| chr22:17199626-17199698 | Common:1; Rare:15 |