| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38681869-38682030 | Common:1; Rare:71 | ||||
| chr22:38739392-38739526 | Common:1; Rare:34 | ||||
| chr22:38739785-38740070 | Rare:75; Clinvar (benign):1 | ||||
| chr22:38742300-38742749 | Common:2; Rare:153; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:38754944-38755070 | Common:4; Rare:28 | ||||
| chr22:38755444-38755562 | Common:1; Rare:24 | ||||
| chr22:39014080-39014291 | Common:1; Rare:51 | ||||
| chr22:39152404-39152785 | Common:5; Rare:120 | ||||
| chr22:39319594-39319715 | Common:3; Rare:65 | ||||
| chr22:39399616-39399802 | Common:3; Rare:72 | ||||
| chr22:39532680-39533041 | Common:2; Rare:140 | ||||
| chr22:40044169-40044362 | Common:2; Rare:42 | ||||
| chr22:40044527-40044861 | Common:2; Rare:79 | ||||
| chr22:40346433-40346655 | Rare:102; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:40463407-40463486 | Rare:14 |