| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42893040-42893336 | Common:4; Rare:97 | ||||
| chr21:44801774-44801870 | Rare:41 | ||||
| chr21:45287879-45288091 | Common:5; Rare:82 | ||||
| chr21:45981546-45981790 | Common:23; Rare:49; Clinvar (benign):2 | ||||
| chr21:46097852-46098163 | Common:3; Rare:95; Clinvar (benign):1 | ||||
| chr21:46286235-46286392 | Common:4; Rare:59 | ||||
| chr21:46323830-46324190 | Common:2; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46635487-46635689 | Common:4; Rare:66 | ||||
| chr22:17628703-17628872 | Common:1; Rare:58 | ||||
| chr22:17638677-17638767 | Rare:28 | ||||
| chr22:18077814-18078006 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19447677-19447914 | Common:2; Rare:96 | ||||
| chr22:19479131-19479473 | Common:4; Rare:121 | ||||
| chr22:19854842-19854972 | Rare:46 | ||||
| chr22:20020880-20021116 | Common:1; Rare:72 |