| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46228717-46228922 | Common:3; Rare:100 | ||||
| chr21:46228980-46229279 | Common:4; Rare:69 | ||||
| chr21:46286004-46286729 | Common:7; Rare:224 | ||||
| chr21:46323262-46323433 | Common:1; Rare:51 | ||||
| chr21:46323786-46324201 | Common:2; Rare:151; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46324368-46324723 | Common:4; Rare:142 | ||||
| chr21:46324839-46324990 | Common:4; Rare:51 | ||||
| chr21:46325220-46325416 | Common:1; Rare:62 | ||||
| chr21:46458435-46459089 | Common:6; Rare:197 | ||||
| chr21:46504272-46504450 | Rare:35 | ||||
| chr21:46635452-46635711 | Common:6; Rare:90 | ||||
| chr21:46635938-46636070 | Common:2; Rare:39 | ||||
| chr22:17084698-17085092 | Common:5; Rare:134; Clinvar:5; Clinvar (benign):3 | ||||
| chr22:17158538-17158718 | Common:2; Rare:36 | ||||
| chr22:17158964-17159122 | Common:2; Rare:45 |