| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:18024899-18024927 | Common:2; Rare:2 | ||||
| chr22:18077799-18078042 | Common:5; Rare:76; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18110650-18110846 | Rare:51 | ||||
| chr22:19122368-19122643 | Common:4; Rare:70 | ||||
| chr22:19144635-19144902 | Common:5; Rare:94 | ||||
| chr22:19178437-19178519 | Common:1; Rare:24 | ||||
| chr22:19291671-19291940 | Common:10; Rare:87 | ||||
| chr22:19432302-19432606 | Common:4; Rare:130 | ||||
| chr22:19447681-19447981 | Common:3; Rare:117 | ||||
| chr22:19479112-19479471 | Common:4; Rare:130 | ||||
| chr22:19524398-19524649 | Common:1; Rare:78 | ||||
| chr22:19854795-19854979 | Rare:63 | ||||
| chr22:19941721-19941891 | Rare:73; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20020923-20021116 | Common:1; Rare:55 | ||||
| chr22:20079948-20080293 | Common:1; Rare:116 |