| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17628648-17628872 | Common:2; Rare:80 | ||||
| chr22:17638689-17638847 | Rare:58 | ||||
| chr22:18024481-18024646 | Common:1; Rare:49 | ||||
| chr22:18077848-18078261 | Common:3; Rare:140; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:18078821-18079103 | Common:2; Rare:63 | ||||
| chr22:18149823-18150213 | Common:2; Rare:90 | ||||
| chr22:19291683-19291900 | Common:10; Rare:76 | ||||
| chr22:19432297-19432567 | Common:3; Rare:111 | ||||
| chr22:19447505-19447836 | Common:2; Rare:151 | ||||
| chr22:19479596-19479949 | Common:5; Rare:82 | ||||
| chr22:19854802-19854988 | Rare:64 | ||||
| chr22:19941765-19941877 | Rare:46; Clinvar:2 | ||||
| chr22:20020873-20021145 | Common:1; Rare:90 | ||||
| chr22:20079936-20080304 | Common:1; Rare:122 | ||||
| chr22:20117175-20117621 | Common:3; Rare:145 |