| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46635598-46635761 | Common:2; Rare:47 | ||||
| chr22:17084824-17085062 | Common:4; Rare:82; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:17159175-17159368 | Common:6; Rare:87 | ||||
| chr22:17628605-17628895 | Common:2; Rare:99 | ||||
| chr22:17706640-17706812 | Common:1; Rare:39 | ||||
| chr22:17876819-17877056 | Common:11; Rare:80 | ||||
| chr22:17877111-17877391 | Common:13; Rare:98 | ||||
| chr22:18024502-18024666 | Rare:52 | ||||
| chr22:18077814-18078058 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19178405-19178519 | Common:1; Rare:35 | ||||
| chr22:19432288-19432610 | Common:4; Rare:139 | ||||
| chr22:19447686-19447967 | Common:2; Rare:108 | ||||
| chr22:19479090-19479466 | Common:4; Rare:136 | ||||
| chr22:19854809-19855061 | Common:1; Rare:95 | ||||
| chr22:19941709-19941900 | Rare:82; Clinvar:6; Clinvar (benign):4 |