| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:28992800-28993045 | Common:1; Rare:112 | ||||
| chr21:31659502-31659752 | Common:2; Rare:118; Clinvar:4; Clinvar (benign):4 | ||||
| chr21:32392993-32393172 | Common:2; Rare:74 | ||||
| chr21:33266262-33266434 | Rare:56; Clinvar:3 | ||||
| chr21:33324705-33325068 | Common:4; Rare:133 | ||||
| chr21:33542810-33543086 | Common:3; Rare:98 | ||||
| chr21:36320052-36320267 | Common:3; Rare:104 | ||||
| chr21:37073015-37073375 | Common:5; Rare:140 | ||||
| chr21:39445765-39445907 | Common:2; Rare:48 | ||||
| chr21:42893040-42893347 | Common:4; Rare:106 | ||||
| chr21:44873668-44874030 | Common:7; Rare:147 | ||||
| chr21:45287879-45288060 | Common:5; Rare:68 | ||||
| chr21:46286081-46286370 | Common:4; Rare:96 | ||||
| chr21:46323830-46324153 | Common:2; Rare:108; Clinvar (benign):1 | ||||
| chr21:46635469-46635726 | Common:5; Rare:87 |