| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31107376-31107721 | Common:2; Rare:114 | ||||
| chr22:31122749-31123002 | Common:3; Rare:64 | ||||
| chr22:31160075-31160232 | Common:1; Rare:55 | ||||
| chr22:31345577-31345630 | Rare:12 | ||||
| chr22:31399394-31399664 | Common:1; Rare:78 | ||||
| chr22:31489737-31490156 | Common:3; Rare:170 | ||||
| chr22:31496077-31496198 | Common:1; Rare:30 | ||||
| chr22:31496406-31496589 | Common:1; Rare:51 | ||||
| chr22:31630782-31631018 | Common:5; Rare:65 | ||||
| chr22:31944297-31944702 | Common:7; Rare:160 | ||||
| chr22:31944743-31944818 | Rare:15 | ||||
| chr22:32412071-32412305 | Common:3; Rare:77 | ||||
| chr22:32475130-32475342 | Common:2; Rare:69; Clinvar (benign):1 | ||||
| chr22:32801525-32801708 | Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:35257465-35257546 | Common:1; Rare:34 |