| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:38498419-38498748 | Common:1; Rare:45 | ||||
| chr21:39183394-39183615 | Common:6; Rare:88 | ||||
| chr21:39348572-39348950 | Common:2; Rare:148 | ||||
| chr21:39445765-39445919 | Common:2; Rare:51 | ||||
| chr21:39451685-39451819 | Rare:30 | ||||
| chr21:39451860-39452139 | Common:3; Rare:91 | ||||
| chr21:42879554-42879665 | Common:2; Rare:28 | ||||
| chr21:42893050-42893371 | Common:4; Rare:113 | ||||
| chr21:42974221-42974619 | Common:1; Rare:154 | ||||
| chr21:43659492-43659623 | Common:1; Rare:40 | ||||
| chr21:43789375-43789602 | Common:1; Rare:77 | ||||
| chr21:44339226-44339469 | Common:2; Rare:74 | ||||
| chr21:45287879-45288118 | Common:5; Rare:89 | ||||
| chr21:45981444-45981946 | Common:24; Rare:134; Clinvar:5; Clinvar (benign):4 | ||||
| chr21:45987017-45987175 | Common:1; Rare:60; Clinvar:9; Clinvar (benign):4 |