| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19178642-19179058 | Common:4; Rare:151; Clinvar (benign):3 | ||||
| chr22:19291653-19291997 | Common:12; Rare:125 | ||||
| chr22:19431688-19432059 | Rare:88 | ||||
| chr22:19432218-19432659 | Common:4; Rare:179 | ||||
| chr22:19447602-19447972 | Common:2; Rare:163 | ||||
| chr22:19448184-19448267 | Rare:18 | ||||
| chr22:19478331-19478622 | Common:4; Rare:59 | ||||
| chr22:19479105-19479466 | Common:4; Rare:132 | ||||
| chr22:19479693-19479995 | Common:4; Rare:87 | ||||
| chr22:19854757-19855215 | Common:6; Rare:158 | ||||
| chr22:19855236-19855295 | Rare:14 | ||||
| chr22:19941387-19941479 | Common:1; Rare:14 | ||||
| chr22:19941680-19941979 | Rare:114; Clinvar:6; Clinvar (benign):7 | ||||
| chr22:19942406-19942543 | Common:4; Rare:28 | ||||
| chr22:20020802-20021217 | Common:2; Rare:126 |