| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:32771707-32772253 | Common:14; Rare:229 | ||||
| chr21:33266275-33266462 | Rare:61; Clinvar:3 | ||||
| chr21:33324858-33325068 | Common:4; Rare:87 | ||||
| chr21:33479854-33480217 | Common:1; Rare:113 | ||||
| chr21:33491704-33491847 | Rare:35 | ||||
| chr21:33542073-33542306 | Common:1; Rare:91 | ||||
| chr21:33542814-33543166 | Common:2; Rare:117 | ||||
| chr21:33588659-33588817 | Rare:74 | ||||
| chr21:33641696-33641944 | Common:1; Rare:63 | ||||
| chr21:33642203-33642545 | Common:1; Rare:134 | ||||
| chr21:36060308-36060613 | Common:5; Rare:84 | ||||
| chr21:36069802-36070053 | Common:7; Rare:72 | ||||
| chr21:36319999-36320267 | Common:3; Rare:127 | ||||
| chr21:36385212-36385440 | Rare:88 | ||||
| chr21:36990191-36990447 | Common:5; Rare:84; Clinvar (benign):4 |