chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98205362282053623CT18GENIChomozygous120279701
98205522482055225GA21GENIChomozygous120279702
98205449482054495AG24GENIChomozygous117587193
98205497882054979TA14GENIChomozygous117587197
98205596382055963C23GENIChomozygous134295445
98205672182056722GC19GENIChomozygous117587204
98205777582057775C9GENIChomozygous134295446
98205839782058397C21GENIChomozygous134295447
98205846882058469TC12GENIChomozygous117587208
98205882282058823CA29GENIChomozygous120279703
98205909482059095AG17GENIChomozygous117587210
98205942882059428CTATTCTTG11GENIChomozygous134295448
98205945182059452GT11GENIChomozygous120279704
98205968682059687AT12GENIChomozygous117587214
98205995682059957AG19GENIChomozygous120279705
98206124582061246AC22GENICpossibly homozygous117587218
98206128582061286GA22GENIChomozygous120279706
98206134382061344TA21GENIChomozygous120279707
98206169282061693AG18GENIChomozygous117587220
98206179782061798TC23GENIChomozygous117587222
98206228382062284GA22GENIChomozygous120279708
98206314282063142CGGAACTTG20GENIChomozygous134295449
98206349482063494T16GENIChomozygous134295450
98206352482063525GT15GENIChomozygous117587226
98206485382064854TA24GENIChomozygous117587232
98206487282064873AG24GENIChomozygous120279709
98206488982064890TA25GENIChomozygous117587234