| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44873605-44874050 | Common:8; Rare:180 | ||||
| chr21:45287867-45288093 | Common:6; Rare:89 | ||||
| chr21:46286256-46286401 | Common:4; Rare:53 | ||||
| chr21:46323871-46324177 | Common:2; Rare:102; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46635457-46635726 | Common:6; Rare:94 | ||||
| chr22:17159175-17159373 | Common:6; Rare:90 | ||||
| chr22:17628616-17628866 | Common:2; Rare:81 | ||||
| chr22:18077857-18078019 | Common:2; Rare:55; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18110619-18110846 | Rare:61 | ||||
| chr22:19291698-19291932 | Common:9; Rare:70 | ||||
| chr22:19432303-19432606 | Common:4; Rare:129 | ||||
| chr22:19941721-19941878 | Rare:67; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20020891-20021167 | Common:1; Rare:92 | ||||
| chr22:20079921-20080249 | Common:1; Rare:103 | ||||
| chr22:20117159-20117571 | Common:3; Rare:133 |