| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:32279513-32279913 | Common:2; Rare:64 | ||||
| chr21:32392870-32393270 | Common:21; Rare:666 | ||||
| chr21:32393287-32393496 | Rare:85 | ||||
| chr21:32393510-32394030 | Common:4; Rare:89 | ||||
| chr21:32411450-32411970 | Common:6; Rare:212 | ||||
| chr21:32428170-32428440 | Common:4; Rare:51 | ||||
| chr21:32587170-32587586 | Common:7; Rare:188 | ||||
| chr21:32604019-32604519 | Common:3; Rare:226; Clinvar:8; Clinvar (benign):4 | ||||
| chr21:32611376-32611776 | Common:3; Rare:109 | ||||
| chr21:32612027-32613099 | Common:5; Rare:963; Clinvar:4; Clinvar (benign):1 | ||||
| chr21:32613119-32613742 | Common:3; Rare:118 | ||||
| chr21:32726784-32727257 | Common:2; Rare:192; Clinvar:6; Clinvar (benign):5 | ||||
| chr21:32727281-32727735 | Common:3; Rare:153 | ||||
| chr21:32727856-32728605 | Common:2; Rare:1037; Clinvar:14 | ||||
| chr21:32770852-32771532 | Rare:274 |