| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45505241-45505390 | Common:2; Rare:83; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr21:45981500-45981813 | Common:23; Rare:71; Clinvar (benign):2 | ||||
| chr21:46184423-46184725 | Common:3; Rare:26 | ||||
| chr21:46259149-46259426 | Common:2; Rare:59 | ||||
| chr21:46286221-46286397 | Common:4; Rare:67 | ||||
| chr21:46323841-46324261 | Common:3; Rare:153; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:46458696-46459090 | Common:4; Rare:135 | ||||
| chr21:46504134-46504417 | Rare:62 | ||||
| chr21:46635487-46635761 | Common:6; Rare:92 | ||||
| chr21:46636169-46636485 | Common:2; Rare:61 | ||||
| chr22:17158976-17159386 | Common:10; Rare:164 | ||||
| chr22:17628604-17628860 | Common:2; Rare:80 | ||||
| chr22:17638689-17638827 | Rare:50 | ||||
| chr22:17774448-17774658 | Rare:66 | ||||
| chr22:18077820-18078026 | Common:4; Rare:67; Clinvar:3; Clinvar (benign):2 |