| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44339226-44339469 | Common:2; Rare:74 | ||||
| chr21:44801706-44801859 | Rare:63 | ||||
| chr21:44873506-44873542 | Rare:12 | ||||
| chr21:44873544-44874061 | Common:9; Rare:197 | ||||
| chr21:44939865-44940042 | Common:3; Rare:48 | ||||
| chr21:45287859-45288082 | Common:6; Rare:90 | ||||
| chr21:45455465-45455783 | Common:5; Rare:135; Clinvar:1; Clinvar (benign):3 | ||||
| chr21:45455789-45455941 | Common:1; Rare:68; Clinvar (benign):1 | ||||
| chr21:45455957-45456248 | Common:4; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46286235-46286397 | Common:4; Rare:60 | ||||
| chr21:46323823-46324231 | Common:3; Rare:151; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458686-46459084 | Common:4; Rare:136 | ||||
| chr22:17159164-17159385 | Common:6; Rare:103 | ||||
| chr22:17569348-17569868 | Common:3; Rare:95 | ||||
| chr22:17628637-17628860 | Common:2; Rare:77 |