| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:32851325-32851557 | Common:2; Rare:34 | ||||
| chr22:32857181-32857384 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:32858912-32859115 | Rare:34 | ||||
| chr22:35330223-35330479 | Common:1; Rare:72 | ||||
| chr22:35390323-35390346 | Rare:4 | ||||
| chr22:36288725-36289301 | Common:2; Rare:174; Clinvar:6; Clinvar (benign):10 | ||||
| chr22:36293762-36294052 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):4 | ||||
| chr22:36305913-36306156 | Common:2; Rare:68; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:36322532-36322848 | Common:1; Rare:78; Clinvar (benign):1 | ||||
| chr22:36326921-36327020 | Rare:17 | ||||
| chr22:36455032-36455329 | Common:3; Rare:98 | ||||
| chr22:36862455-36862558 | Common:1; Rare:21 | ||||
| chr22:36867334-36867417 | Rare:27 | ||||
| chr22:37228543-37228577 | Rare:9 | ||||
| chr22:37747240-37747659 | Rare:97 |