| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45073800-45073840 | Common:2; Rare:17 | ||||
| chr21:45287867-45288093 | Common:6; Rare:89 | ||||
| chr21:45981519-45981841 | Common:23; Rare:79; Clinvar (benign):2 | ||||
| chr21:46184418-46184783 | Common:4; Rare:35 | ||||
| chr21:46228750-46228959 | Common:4; Rare:95 | ||||
| chr21:46286233-46286402 | Common:4; Rare:63 | ||||
| chr21:46286586-46286684 | Common:1; Rare:35 | ||||
| chr21:46323770-46324206 | Common:2; Rare:161; Clinvar:3; Clinvar (benign):1 | ||||
| chr21:46635497-46635747 | Common:5; Rare:84 | ||||
| chr22:17159175-17159393 | Common:6; Rare:108 | ||||
| chr22:17628653-17628872 | Common:2; Rare:79 | ||||
| chr22:17638684-17638818 | Rare:46 | ||||
| chr22:17774398-17774569 | Rare:58 | ||||
| chr22:18077829-18078022 | Common:4; Rare:64; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18149763-18150000 | Common:1; Rare:41 |