| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42980377-42980557 | Common:3; Rare:27 | ||||
| chr21:43262504-43262538 | |||||
| chr21:43262561-43262783 | |||||
| chr21:43332113-43332479 | Common:2; Rare:89 | ||||
| chr21:43362460-43362551 | Rare:25 | ||||
| chr21:43660694-43660803 | Common:1; Rare:30 | ||||
| chr21:43674664-43674728 | Rare:13 | ||||
| chr21:43684589-43684729 | Rare:29 | ||||
| chr21:43865886-43866015 | Common:1; Rare:28 | ||||
| chr21:43894011-43894081 | Common:1; Rare:13 | ||||
| chr21:44034357-44034383 | Rare:5 | ||||
| chr21:44062050-44062300 | Common:1; Rare:36 | ||||
| chr21:44308167-44308188 | Rare:3 | ||||
| chr21:44311070-44311118 | Rare:13 | ||||
| chr21:44313654-44314073 | Common:4; Rare:129; Clinvar (benign):2 |