| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19854791-19854988 | Rare:66 | ||||
| chr22:19941728-19941886 | Rare:67; Clinvar:4; Clinvar (benign):4 | ||||
| chr22:20020892-20021134 | Common:1; Rare:78 | ||||
| chr22:20079930-20080258 | Common:1; Rare:106 | ||||
| chr22:20117185-20117616 | Common:3; Rare:136 | ||||
| chr22:20319998-20320160 | Common:1; Rare:54 | ||||
| chr22:20495771-20495958 | Common:2; Rare:71 | ||||
| chr22:20917138-20917413 | Rare:95 | ||||
| chr22:20982183-20982358 | Common:2; Rare:43; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002088-21002251 | Common:4; Rare:59 | ||||
| chr22:21567642-21567768 | Common:1; Rare:48 | ||||
| chr22:21938085-21938345 | Rare:83 | ||||
| chr22:21982754-21982897 | Rare:35 | ||||
| chr22:23145183-23145522 | Common:3; Rare:114 | ||||
| chr22:23762952-23763021 | Rare:18 |