| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46286492-46286660 | Common:1; Rare:48 | ||||
| chr21:46323868-46324161 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46458686-46459032 | Common:3; Rare:120 | ||||
| chr21:46635472-46635731 | Common:5; Rare:84 | ||||
| chr22:17628706-17628895 | Common:1; Rare:68 | ||||
| chr22:17638593-17638878 | Rare:97 | ||||
| chr22:17774390-17774580 | Rare:65 | ||||
| chr22:19447706-19447866 | Common:2; Rare:52 | ||||
| chr22:19854838-19854983 | Rare:49 | ||||
| chr22:19941717-19941878 | Rare:70; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20080018-20080288 | Rare:94 | ||||
| chr22:20117212-20117563 | Common:3; Rare:111 | ||||
| chr22:20319995-20320158 | Common:2; Rare:53 | ||||
| chr22:20495787-20495994 | Common:2; Rare:77 | ||||
| chr22:20582933-20583238 | Rare:88 |