| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:33542771-33543167 | Common:4; Rare:133 | ||||
| chr21:33641683-33641980 | Common:1; Rare:81 | ||||
| chr21:33642170-33642705 | Common:2; Rare:190 | ||||
| chr21:34073486-34073741 | Rare:115 | ||||
| chr21:36060238-36060678 | Common:7; Rare:129 | ||||
| chr21:36069906-36070041 | Common:6; Rare:42 | ||||
| chr21:36319972-36320273 | Common:4; Rare:143 | ||||
| chr21:36966349-36966596 | Common:2; Rare:73 | ||||
| chr21:36990181-36990287 | Common:4; Rare:37; Clinvar (benign):4 | ||||
| chr21:37072511-37072805 | Common:8; Rare:139; Clinvar (pathogenic):1 | ||||
| chr21:37072989-37073442 | Common:5; Rare:164 | ||||
| chr21:37267296-37267730 | Common:4; Rare:155 | ||||
| chr21:37268074-37268138 | Common:1; Rare:14 | ||||
| chr21:39313447-39313921 | Common:9; Rare:256 | ||||
| chr21:39314279-39314486 | Common:3; Rare:104 |