| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:39445817-39445919 | Common:1; Rare:35 | ||||
| chr21:41361968-41362030 | Rare:8 | ||||
| chr21:42893066-42893342 | Common:4; Rare:93 | ||||
| chr21:44873563-44874043 | Common:8; Rare:189 | ||||
| chr21:45287864-45288093 | Common:6; Rare:90 | ||||
| chr21:45981513-45981946 | Common:24; Rare:114; Clinvar:5; Clinvar (benign):4 | ||||
| chr21:45986941-45987175 | Common:2; Rare:90; Clinvar:20; Clinvar (benign):8 | ||||
| chr21:46002215-46002710 | Common:3; Rare:158; Clinvar:21; Clinvar (benign):14 | ||||
| chr21:46184406-46184747 | Common:4; Rare:32 | ||||
| chr21:46286268-46286370 | Common:2; Rare:36 | ||||
| chr21:46323863-46324153 | Common:2; Rare:98; Clinvar (benign):1 | ||||
| chr21:46635487-46635693 | Common:5; Rare:67 | ||||
| chr22:17159207-17159385 | Common:4; Rare:87 | ||||
| chr22:17628690-17628966 | Common:1; Rare:96 | ||||
| chr22:18077820-18078006 | Common:3; Rare:62; Clinvar:3; Clinvar (benign):1 |