| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46286230-46286697 | Common:6; Rare:159 | ||||
| chr21:46323774-46324225 | Common:3; Rare:174; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458662-46459123 | Common:4; Rare:157 | ||||
| chr21:46635457-46635766 | Common:7; Rare:106 | ||||
| chr22:17084812-17085043 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:17628613-17628882 | Common:2; Rare:92 | ||||
| chr22:17638485-17638882 | Common:1; Rare:112 | ||||
| chr22:17774383-17774539 | Rare:51 | ||||
| chr22:17877278-17877535 | Common:13; Rare:72 | ||||
| chr22:18024508-18024612 | Rare:30 | ||||
| chr22:18077820-18078058 | Common:4; Rare:76; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19178405-19178526 | Common:1; Rare:36 | ||||
| chr22:19291700-19291907 | Common:9; Rare:68 | ||||
| chr22:19447690-19447929 | Common:2; Rare:92 | ||||
| chr22:19479093-19479466 | Common:4; Rare:136 |