| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:18077980-18078014 | Rare:11; Clinvar:2 | ||||
| chr22:18150040-18150181 | Common:1; Rare:37 | ||||
| chr22:19291717-19291893 | Common:9; Rare:54 | ||||
| chr22:19432269-19432591 | Common:4; Rare:135 | ||||
| chr22:19447677-19447788 | Common:1; Rare:52 | ||||
| chr22:19479116-19479463 | Common:4; Rare:123 | ||||
| chr22:19479661-19479963 | Common:5; Rare:82 | ||||
| chr22:19854791-19854990 | Rare:67 | ||||
| chr22:19881149-19881506 | Common:4; Rare:96 | ||||
| chr22:19941746-19941886 | Rare:56; Clinvar:4 | ||||
| chr22:20020864-20021141 | Common:1; Rare:90 | ||||
| chr22:20079930-20080293 | Common:1; Rare:119 | ||||
| chr22:20117163-20117652 | Common:4; Rare:160 | ||||
| chr22:20319998-20320160 | Common:1; Rare:54 | ||||
| chr22:20982196-20982358 | Common:2; Rare:37; Clinvar (benign):2; Clinvar (pathogenic):1 |