| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46053597-46053863 | Rare:87 | ||||
| chr22:46250268-46250413 | Common:2; Rare:46 | ||||
| chr22:46267870-46268027 | Common:1; Rare:47 | ||||
| chr22:46296745-46296924 | Rare:59 | ||||
| chr22:46335614-46335760 | Common:2; Rare:62; Clinvar:5; Clinvar (benign):6 | ||||
| chr22:46762476-46762669 | Common:3; Rare:73 | ||||
| chr22:49853601-49853915 | Common:2; Rare:113 | ||||
| chr22:50270327-50270623 | Common:1; Rare:87 | ||||
| chr22:50525531-50525619 | Common:3; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50582404-50582608 | Common:1; Rare:101; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:50582788-50583132 | Common:7; Rare:109; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628139-50628276 | Common:7; Rare:68; Clinvar:1 | ||||
| chr22:50783574-50783853 | Common:2; Rare:94 | ||||
| chr3:196352-196614 | Common:1; Rare:65 | ||||
| chr3:196707-197074 | Common:2; Rare:120 |