| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42893064-42893336 | Common:4; Rare:88 | ||||
| chr21:43020874-43021145 | Common:1; Rare:51 | ||||
| chr21:43659468-43659631 | Common:1; Rare:54 | ||||
| chr21:43728603-43728878 | Common:3; Rare:69 | ||||
| chr21:43776228-43776657 | Common:5; Rare:152; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr21:43789378-43789610 | Common:1; Rare:83 | ||||
| chr21:44801765-44801876 | Rare:48 | ||||
| chr21:44873673-44874050 | Common:7; Rare:152 | ||||
| chr21:44928653-44928893 | Common:9; Rare:41 | ||||
| chr21:44931935-44932020 | Rare:18 | ||||
| chr21:45287875-45288049 | Common:6; Rare:67 | ||||
| chr21:46184423-46184705 | Common:3; Rare:24 | ||||
| chr21:46286233-46286402 | Common:4; Rare:63 | ||||
| chr21:46323821-46324203 | Common:2; Rare:136; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:17628706-17628866 | Common:1; Rare:51 |