| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:32392959-32393191 | Common:4; Rare:99 | ||||
| chr21:32612319-32612910 | Rare:146 | ||||
| chr21:33266268-33266434 | Rare:55; Clinvar:3 | ||||
| chr21:33324844-33325082 | Common:4; Rare:101 | ||||
| chr21:33479820-33480023 | Rare:76 | ||||
| chr21:33542077-33542232 | Rare:61 | ||||
| chr21:33542812-33543101 | Common:3; Rare:105 | ||||
| chr21:33641704-33641898 | Common:1; Rare:48 | ||||
| chr21:33642201-33642545 | Common:1; Rare:134 | ||||
| chr21:34526760-34527115 | Common:2; Rare:69 | ||||
| chr21:36060489-36060607 | Common:1; Rare:37 | ||||
| chr21:36069782-36070068 | Common:7; Rare:80 | ||||
| chr21:36134938-36135086 | Rare:39 | ||||
| chr21:36320012-36320258 | Common:3; Rare:118 | ||||
| chr21:37072508-37072705 | Common:5; Rare:102; Clinvar (pathogenic):1 |