| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:14383082-14383493 | Common:2; Rare:116 | ||||
| chr21:17512772-17513127 | Common:2; Rare:115 | ||||
| chr21:17612814-17613098 | Common:1; Rare:128 | ||||
| chr21:17819181-17819488 | Common:1; Rare:106 | ||||
| chr21:17819672-17819689 | Rare:7 | ||||
| chr21:25607458-25607622 | Rare:79 | ||||
| chr21:25734832-25735132 | Common:2; Rare:116 | ||||
| chr21:25735144-25735282 | Rare:51 | ||||
| chr21:25735290-25735489 | Common:3; Rare:52 | ||||
| chr21:25735527-25735792 | Common:1; Rare:63 | ||||
| chr21:26170639-26170946 | Common:6; Rare:100; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:26845261-26845641 | Common:2; Rare:109 | ||||
| chr21:28992789-28993103 | Common:2; Rare:131 | ||||
| chr21:29019307-29019400 | Common:5; Rare:41 | ||||
| chr21:29024526-29024726 | Common:2; Rare:86 |