| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29024534-29024773 | Common:2; Rare:103 | ||||
| chr21:29024845-29025008 | Rare:33 | ||||
| chr21:29073230-29073437 | Common:1; Rare:55 | ||||
| chr21:29073523-29073865 | Common:2; Rare:104 | ||||
| chr21:29145423-29145690 | Rare:41 | ||||
| chr21:29298755-29298960 | Common:2; Rare:88 | ||||
| chr21:29299079-29299538 | Common:2; Rare:138 | ||||
| chr21:29300112-29300421 | Common:2; Rare:71 | ||||
| chr21:31659502-31659837 | Common:2; Rare:150; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31659983-31660181 | Rare:50 | ||||
| chr21:32279013-32279214 | Common:3; Rare:85 | ||||
| chr21:32392946-32393187 | Common:3; Rare:104 | ||||
| chr21:32612353-32612728 | Rare:89 | ||||
| chr21:32726779-32727039 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):3 | ||||
| chr21:32727893-32728105 | Rare:106; Clinvar:2 |