| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63707875-63708086 | Rare:62 | ||||
| chr20:63865002-63865366 | Common:2; Rare:129 | ||||
| chr21:17819327-17819463 | Common:1; Rare:47 | ||||
| chr21:25607458-25607555 | Rare:54 | ||||
| chr21:25734859-25735463 | Common:4; Rare:212 | ||||
| chr21:25735608-25735923 | Common:4; Rare:84 | ||||
| chr21:26842916-26843128 | Common:4; Rare:40 | ||||
| chr21:26845401-26845555 | Common:1; Rare:38 | ||||
| chr21:29024467-29024726 | Common:3; Rare:103 | ||||
| chr21:29298734-29298930 | Common:1; Rare:83 | ||||
| chr21:31659531-31659838 | Common:2; Rare:132; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:32279028-32279205 | Common:3; Rare:76 | ||||
| chr21:32392965-32393163 | Common:2; Rare:85 | ||||
| chr21:32771844-32772161 | Common:12; Rare:130 | ||||
| chr21:33266255-33266434 | Rare:56; Clinvar:3 |