| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50507610-50507961 | Common:1; Rare:108 | ||||
| chr22:50508216-50508351 | Rare:47 | ||||
| chr22:50508432-50508563 | Common:2; Rare:39 | ||||
| chr22:50525123-50525405 | Common:2; Rare:88 | ||||
| chr22:50525432-50526077 | Common:10; Rare:298; Clinvar:8; Clinvar (benign):13; Clinvar (pathogenic):4 | ||||
| chr22:50526092-50526609 | Common:4; Rare:263; Clinvar:9; Clinvar (benign):10; Clinvar (pathogenic):7 | ||||
| chr22:50526842-50527211 | Common:1; Rare:121; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:50529974-50530516 | Common:2; Rare:173; Clinvar:3 | ||||
| chr22:50530911-50531294 | Common:1; Rare:137 | ||||
| chr22:50531505-50532032 | Common:3; Rare:136 | ||||
| chr22:50532433-50532715 | Common:2; Rare:68 | ||||
| chr22:50548475-50548595 | Rare:44 | ||||
| chr22:50562729-50563119 | Common:6; Rare:98 | ||||
| chr22:50582177-50582280 | Common:1; Rare:33; Clinvar (benign):2 | ||||
| chr22:50582308-50582403 | Rare:31; Clinvar:2; Clinvar (benign):1 |