| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44886799-44887196 | Common:3; Rare:101; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr21:44931207-44931468 | Common:2; Rare:57 | ||||
| chr21:45349863-45350142 | Common:1; Rare:48 | ||||
| chr21:45492290-45492564 | Common:1; Rare:76; Clinvar (benign):2 | ||||
| chr21:45496294-45496535 | Rare:80 | ||||
| chr21:45509817-45510261 | Common:6; Rare:190; Clinvar:3; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr21:45512055-45512366 | Common:2; Rare:126; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr21:45535762-45535906 | Rare:34 | ||||
| chr21:45917264-45917447 | Rare:40 | ||||
| chr21:46121932-46122158 | Common:3; Rare:84; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr21:46240948-46241132 | Common:1; Rare:57 | ||||
| chr21:46243651-46243797 | Rare:50 | ||||
| chr21:46266240-46266369 | Common:2; Rare:22 | ||||
| chr21:46366431-46366672 | Common:3; Rare:64; Clinvar:4; Clinvar (benign):3 | ||||
| chr21:46437991-46438256 | Rare:64; Clinvar:4 |