| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46635470-46635731 | Common:5; Rare:86 | ||||
| chr22:17159167-17159385 | Common:6; Rare:102 | ||||
| chr22:17569643-17569682 | Rare:8 | ||||
| chr22:17628699-17628848 | Common:1; Rare:48 | ||||
| chr22:17638663-17638817 | Rare:53 | ||||
| chr22:17774394-17774536 | Rare:45 | ||||
| chr22:18077814-18078038 | Common:4; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18149818-18150191 | Common:2; Rare:86 | ||||
| chr22:19178449-19178510 | Common:1; Rare:15 | ||||
| chr22:19291671-19291964 | Common:10; Rare:96 | ||||
| chr22:19432294-19432606 | Common:4; Rare:134 | ||||
| chr22:19447667-19447729 | Rare:43 | ||||
| chr22:19524390-19524660 | Common:1; Rare:83 | ||||
| chr22:19854795-19854999 | Rare:72 | ||||
| chr22:19941733-19941882 | Rare:61; Clinvar:4; Clinvar (benign):3 |