| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44353472-44353644 | Common:2; Rare:31 | ||||
| chr21:44801739-44801977 | Common:1; Rare:94 | ||||
| chr21:44817626-44818299 | Common:19; Rare:262 | ||||
| chr21:44873571-44874134 | Common:9; Rare:210 | ||||
| chr21:44920128-44920433 | Common:4; Rare:80 | ||||
| chr21:44920812-44921144 | Common:1; Rare:85; Clinvar:4; Clinvar (benign):1 | ||||
| chr21:44921373-44921446 | Rare:12 | ||||
| chr21:44928458-44928685 | Common:1; Rare:80 | ||||
| chr21:44931179-44931742 | Common:3; Rare:137 | ||||
| chr21:44939799-44940092 | Common:4; Rare:72 | ||||
| chr21:45074419-45074580 | Common:2; Rare:82 | ||||
| chr21:45287820-45288108 | Common:6; Rare:114 | ||||
| chr21:45541794-45541998 | Common:2; Rare:55 | ||||
| chr21:45542391-45542624 | Rare:65 | ||||
| chr21:46184409-46184768 | Common:4; Rare:34 |