| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63969837-63970089 | Common:3; Rare:87 | ||||
| chr20:64062951-64063319 | Common:3; Rare:133 | ||||
| chr20:64079903-64080115 | Common:2; Rare:85 | ||||
| chr21:14383115-14383493 | Common:2; Rare:104 | ||||
| chr21:15064836-15065133 | Rare:94 | ||||
| chr21:17512549-17512851 | Common:4; Rare:80 | ||||
| chr21:17512894-17513139 | Common:1; Rare:85 | ||||
| chr21:17612827-17613056 | Common:1; Rare:104 | ||||
| chr21:17819324-17819421 | Common:1; Rare:35 | ||||
| chr21:17819664-17819689 | Rare:10 | ||||
| chr21:25607468-25607555 | Rare:47 | ||||
| chr21:25734832-25735506 | Common:5; Rare:228 | ||||
| chr21:25735525-25735721 | Rare:55 | ||||
| chr21:25735742-25735931 | Common:4; Rare:48 | ||||
| chr21:26170562-26170928 | Common:6; Rare:119; Clinvar:5; Clinvar (benign):2 |