| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45986935-45987175 | Common:2; Rare:93; Clinvar:20; Clinvar (benign):8 | ||||
| chr21:46002216-46002698 | Common:2; Rare:153; Clinvar:21; Clinvar (benign):13 | ||||
| chr21:46097554-46097635 | Common:3; Rare:18 | ||||
| chr21:46323841-46324159 | Common:2; Rare:106; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:17628712-17628916 | Common:1; Rare:74 | ||||
| chr22:17638677-17638811 | Rare:46 | ||||
| chr22:18077802-18078007 | Common:4; Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19291707-19291917 | Common:9; Rare:64 | ||||
| chr22:19432303-19432567 | Common:3; Rare:106 | ||||
| chr22:19941722-19941886 | Rare:69; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20319999-20320178 | Common:1; Rare:61 | ||||
| chr22:20495787-20495904 | Common:1; Rare:43 | ||||
| chr22:20982215-20982358 | Common:1; Rare:30; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:21002092-21002215 | Common:3; Rare:47 | ||||
| chr22:21938234-21938298 | Rare:29 |