| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:37073006-37073375 | Common:5; Rare:143 | ||||
| chr21:37267296-37267676 | Common:4; Rare:135 | ||||
| chr21:39380242-39380487 | Common:1; Rare:119 | ||||
| chr21:39387657-39387817 | Common:2; Rare:71 | ||||
| chr21:39445751-39445919 | Common:3; Rare:55 | ||||
| chr21:41426096-41426263 | Common:3; Rare:38 | ||||
| chr21:41879320-41879563 | Common:5; Rare:79 | ||||
| chr21:42893072-42893342 | Common:3; Rare:92 | ||||
| chr21:42974231-42974649 | Common:1; Rare:155 | ||||
| chr21:43659461-43659566 | Common:1; Rare:35 | ||||
| chr21:43789377-43789617 | Common:1; Rare:87 | ||||
| chr21:44339226-44339469 | Common:2; Rare:74 | ||||
| chr21:44873600-44874040 | Common:8; Rare:177 | ||||
| chr21:45287867-45288102 | Common:6; Rare:92 | ||||
| chr21:45981500-45981901 | Common:24; Rare:102; Clinvar:3; Clinvar (benign):3 |