| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31748964-31749491 | Common:2; Rare:159 | ||||
| chr22:31753042-31753329 | Rare:56 | ||||
| chr22:31857251-31857751 | Common:2; Rare:239; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr22:31887511-31887661 | Rare:29 | ||||
| chr22:31893547-31893772 | Rare:62; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:31926950-31927320 | Common:3; Rare:53 | ||||
| chr22:31963915-31964315 | Common:3; Rare:97 | ||||
| chr22:31970547-31970947 | Common:11; Rare:151 | ||||
| chr22:32204820-32205310 | Common:4; Rare:106 | ||||
| chr22:32622579-32622709 | Rare:18 | ||||
| chr22:32977678-32978078 | Common:3; Rare:98 | ||||
| chr22:32986101-32986306 | Common:1; Rare:47 | ||||
| chr22:32987020-32987400 | Common:2; Rare:70 | ||||
| chr22:32993922-32994138 | Common:2; Rare:46 | ||||
| chr22:32995078-32995181 | Rare:19 |