| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44801774-44801876 | Rare:42 | ||||
| chr21:44873605-44874050 | Common:8; Rare:180 | ||||
| chr21:45287879-45288102 | Common:5; Rare:85 | ||||
| chr21:45981519-45981824 | Common:23; Rare:70; Clinvar (benign):2 | ||||
| chr21:45987017-45987175 | Common:1; Rare:60; Clinvar:9; Clinvar (benign):4 | ||||
| chr21:46184423-46184736 | Common:4; Rare:28 | ||||
| chr21:46286235-46286396 | Common:4; Rare:60 | ||||
| chr21:46323871-46324203 | Common:2; Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46458671-46459108 | Common:4; Rare:148 | ||||
| chr21:46635492-46635735 | Common:5; Rare:79 | ||||
| chr22:17159190-17159375 | Common:5; Rare:84 | ||||
| chr22:17628601-17628866 | Common:2; Rare:83 | ||||
| chr22:17638684-17638827 | Rare:51 | ||||
| chr22:18077820-18078022 | Common:4; Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19291671-19291930 | Common:10; Rare:82 |