| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43812223-43812500 | Common:4; Rare:95 | ||||
| chr22:43862401-43862635 | Common:8; Rare:91 | ||||
| chr22:43955253-43955566 | Common:4; Rare:92 | ||||
| chr22:44024116-44024406 | Common:2; Rare:90 | ||||
| chr22:44026302-44026335 | Rare:9 | ||||
| chr22:45163654-45164023 | Common:4; Rare:133 | ||||
| chr22:45309712-45309983 | Common:1; Rare:103 | ||||
| chr22:45329429-45329730 | Common:4; Rare:85 | ||||
| chr22:45413564-45413762 | Common:1; Rare:81 | ||||
| chr22:45671758-45672108 | Common:3; Rare:137 | ||||
| chr22:46053722-46053901 | Rare:67 | ||||
| chr22:46250240-46250413 | Common:3; Rare:50 | ||||
| chr22:46267841-46268042 | Common:1; Rare:65 | ||||
| chr22:46296672-46296924 | Common:2; Rare:90 | ||||
| chr22:46335598-46335943 | Common:8; Rare:157; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):2 |