| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:17512898-17513067 | Rare:60 | ||||
| chr21:17612872-17613107 | Rare:109 | ||||
| chr21:17819313-17819732 | Common:2; Rare:138 | ||||
| chr21:25607086-25607267 | Rare:38 | ||||
| chr21:25607458-25607636 | Rare:83 | ||||
| chr21:25639114-25639290 | Common:2; Rare:38 | ||||
| chr21:25639449-25639644 | Rare:47 | ||||
| chr21:25639690-25640050 | Common:6; Rare:177 | ||||
| chr21:25734836-25735065 | Common:2; Rare:98 | ||||
| chr21:25735333-25735461 | Common:1; Rare:35 | ||||
| chr21:25735500-25735850 | Common:3; Rare:82 | ||||
| chr21:26168980-26169370 | Rare:77 | ||||
| chr21:26169663-26170175 | Common:4; Rare:137 | ||||
| chr21:26170677-26170897 | Common:3; Rare:74; Clinvar:4; Clinvar (benign):2 | ||||
| chr21:26572720-26572930 | Common:1; Rare:52 |