| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45493103-45493206 | Rare:42 | ||||
| chr21:45505075-45505388 | Common:5; Rare:170; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr21:45981500-45981897 | Common:24; Rare:102; Clinvar:3; Clinvar (benign):3 | ||||
| chr21:45986713-45987008 | Common:4; Rare:90; Clinvar:11; Clinvar (benign):5 | ||||
| chr21:46001957-46002288 | Common:2; Rare:118; Clinvar:12; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr21:46097806-46098167 | Common:4; Rare:110; Clinvar (benign):1 | ||||
| chr21:46184423-46184697 | Common:3; Rare:24 | ||||
| chr21:46286209-46286402 | Common:4; Rare:73 | ||||
| chr21:46323868-46324238 | Common:3; Rare:139; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46324459-46324686 | Common:4; Rare:83 | ||||
| chr21:46458652-46459063 | Common:3; Rare:142 | ||||
| chr21:46635472-46635744 | Common:5; Rare:89 | ||||
| chr22:17159183-17159375 | Common:5; Rare:85 | ||||
| chr22:17563243-17563501 | Common:2; Rare:54 | ||||
| chr22:17628675-17628980 | Common:1; Rare:109 |