| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45981522-45981829 | Common:23; Rare:70; Clinvar (benign):2 | ||||
| chr21:46184409-46184764 | Common:4; Rare:32 | ||||
| chr21:46285987-46286412 | Common:5; Rare:129 | ||||
| chr21:46286580-46286673 | Common:1; Rare:31 | ||||
| chr21:46323784-46324225 | Common:3; Rare:170; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46324459-46324686 | Common:4; Rare:83 | ||||
| chr21:46635115-46635171 | Rare:6 | ||||
| chr21:46635487-46635731 | Common:5; Rare:81 | ||||
| chr22:17159167-17159402 | Common:6; Rare:116 | ||||
| chr22:17628697-17628906 | Common:1; Rare:75 | ||||
| chr22:17638677-17638827 | Rare:54 | ||||
| chr22:17773741-17773830 | Common:1; Rare:17 | ||||
| chr22:17773889-17773966 | Rare:23 | ||||
| chr22:17774383-17774560 | Rare:61 | ||||
| chr22:18077785-18078022 | Common:5; Rare:73; Clinvar:3; Clinvar (benign):2 |