| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63980987-63981224 | Common:4; Rare:78; Clinvar:7; Clinvar (benign):4 | ||||
| chr21:14383111-14383321 | Common:1; Rare:65 | ||||
| chr21:17512818-17513120 | Common:2; Rare:103 | ||||
| chr21:17819305-17819434 | Common:1; Rare:50 | ||||
| chr21:25607458-25607577 | Rare:62 | ||||
| chr21:25734865-25735435 | Common:3; Rare:203 | ||||
| chr21:25735531-25735792 | Common:1; Rare:61 | ||||
| chr21:26170710-26170890 | Common:3; Rare:64; Clinvar:4; Clinvar (benign):2 | ||||
| chr21:26573113-26573336 | Rare:71 | ||||
| chr21:28992809-28993110 | Common:2; Rare:128 | ||||
| chr21:29019312-29019434 | Common:5; Rare:48 | ||||
| chr21:29024520-29024726 | Common:2; Rare:86 | ||||
| chr21:29024876-29024991 | Rare:20 | ||||
| chr21:29073592-29073865 | Common:2; Rare:80 | ||||
| chr21:29298749-29298930 | Common:1; Rare:76 |