| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:45671989-45672066 | Rare:35 | ||||
| chr22:46053592-46053885 | Rare:94 | ||||
| chr22:46250268-46250394 | Common:1; Rare:39 | ||||
| chr22:46267870-46268027 | Common:1; Rare:47 | ||||
| chr22:46335614-46335770 | Common:2; Rare:68; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:46762496-46762669 | Common:3; Rare:64 | ||||
| chr22:50244488-50244637 | Common:1; Rare:46 | ||||
| chr22:50244954-50245076 | Common:2; Rare:47 | ||||
| chr22:50525538-50525685 | Common:3; Rare:74; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50628139-50628276 | Common:7; Rare:68; Clinvar:1 | ||||
| chr22:50783576-50783859 | Common:2; Rare:95 | ||||
| chr3:196468-196614 | Rare:38 | ||||
| chr3:196707-197054 | Common:2; Rare:112 | ||||
| chr3:197194-197354 | Rare:48 | ||||
| chr3:197537-198038 | Common:7; Rare:188 |