| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45981500-45981813 | Common:23; Rare:71; Clinvar (benign):2 | ||||
| chr21:46323837-46324153 | Common:2; Rare:105; Clinvar (benign):1 | ||||
| chr21:46635542-46635726 | Common:1; Rare:57 | ||||
| chr22:17628706-17628872 | Common:1; Rare:56 | ||||
| chr22:17638677-17638811 | Rare:46 | ||||
| chr22:19432345-19432606 | Common:2; Rare:112 | ||||
| chr22:19479687-19479956 | Common:4; Rare:72 | ||||
| chr22:19941653-19941878 | Rare:95; Clinvar:6; Clinvar (benign):7 | ||||
| chr22:20079936-20080287 | Common:1; Rare:115 | ||||
| chr22:20117246-20117571 | Common:3; Rare:104 | ||||
| chr22:20320009-20320158 | Common:1; Rare:50 | ||||
| chr22:21002060-21002195 | Common:3; Rare:50 | ||||
| chr22:21642064-21642355 | Common:2; Rare:86 | ||||
| chr22:21665928-21666047 | Rare:32 | ||||
| chr22:23974407-23974689 | Common:1; Rare:4 |