| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63980969-63981266 | Common:4; Rare:94; Clinvar:7; Clinvar (benign):4 | ||||
| chr21:25607458-25607560 | Rare:56 | ||||
| chr21:25734851-25735066 | Common:2; Rare:95 | ||||
| chr21:25735313-25735435 | Rare:32 | ||||
| chr21:25735527-25735676 | Rare:42 | ||||
| chr21:26845407-26845555 | Common:1; Rare:35 | ||||
| chr21:28992801-28993152 | Common:2; Rare:143 | ||||
| chr21:29019312-29019400 | Common:5; Rare:37 | ||||
| chr21:29024508-29024738 | Common:3; Rare:95 | ||||
| chr21:31659514-31659787 | Common:2; Rare:122; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr21:32278999-32279214 | Common:3; Rare:94 | ||||
| chr21:32392965-32393179 | Common:2; Rare:92 | ||||
| chr21:33324881-33325058 | Common:4; Rare:76 | ||||
| chr21:33479854-33480143 | Rare:101 | ||||
| chr21:33542073-33542216 | Rare:52 |