| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46267841-46268038 | Common:1; Rare:62 | ||||
| chr22:46296745-46297036 | Common:2; Rare:90 | ||||
| chr22:46335601-46335966 | Common:8; Rare:164; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr22:46762447-46762701 | Common:3; Rare:96 | ||||
| chr22:49853626-49853899 | Common:2; Rare:99 | ||||
| chr22:49918408-49918702 | Common:1; Rare:109 | ||||
| chr22:50185644-50185988 | Common:6; Rare:128 | ||||
| chr22:50244516-50244669 | Common:1; Rare:49 | ||||
| chr22:50244986-50245076 | Common:1; Rare:36 | ||||
| chr22:50525524-50525728 | Common:5; Rare:102; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50562887-50563044 | Common:3; Rare:45 | ||||
| chr22:50582784-50583145 | Common:7; Rare:122; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628093-50628276 | Common:9; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783592-50783859 | Common:2; Rare:87 | ||||
| chr3:2098583-2098962 | Common:4; Rare:151 |