| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46097781-46098166 | Common:4; Rare:118; Clinvar (benign):1 | ||||
| chr21:46323884-46324231 | Common:3; Rare:132; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458714-46459012 | Common:3; Rare:101 | ||||
| chr22:17628689-17628840 | Common:1; Rare:51 | ||||
| chr22:17638681-17638767 | Rare:26 | ||||
| chr22:18077814-18078022 | Common:4; Rare:67; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19122382-19122588 | Common:4; Rare:56 | ||||
| chr22:19432308-19432557 | Common:3; Rare:98 | ||||
| chr22:19447684-19447836 | Common:1; Rare:60 | ||||
| chr22:19854791-19854997 | Rare:71 | ||||
| chr22:19941575-19941886 | Common:1; Rare:119; Clinvar:6; Clinvar (benign):7 | ||||
| chr22:20020899-20021167 | Common:1; Rare:90 | ||||
| chr22:20117240-20117577 | Common:3; Rare:108 | ||||
| chr22:20319998-20320158 | Common:1; Rare:53 | ||||
| chr22:20495781-20495913 | Common:1; Rare:50 |