| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:45671982-45672076 | Rare:42 | ||||
| chr22:46053742-46053901 | Rare:60 | ||||
| chr22:46250245-46250423 | Common:3; Rare:57 | ||||
| chr22:46267836-46268032 | Common:1; Rare:58 | ||||
| chr22:46335621-46335801 | Common:5; Rare:82; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762503-46762669 | Common:3; Rare:60 | ||||
| chr22:49918277-49918675 | Common:4; Rare:129; Clinvar (benign):3 | ||||
| chr22:50185619-50185949 | Common:6; Rare:120 | ||||
| chr22:50244973-50245114 | Common:1; Rare:57 | ||||
| chr22:50525531-50525697 | Common:4; Rare:79; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50577366-50577645 | Common:2; Rare:78 | ||||
| chr22:50582794-50583142 | Common:7; Rare:114; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628069-50628280 | Common:9; Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783601-50783859 | Common:2; Rare:79 | ||||
| chr3:196702-196914 | Common:1; Rare:67 |