chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4132070173132070174CT8GENIChomozygous126052938
4132071096132071097GT6GENIChomozygous113384085
4132071097132071098AT5GENIChomozygous113384087
4132071118132071119TC9GENIChomozygous112830811
4132071223132071224GA23GENIChomozygous113384089
4132071405132071406GC15GENIChomozygous113384091
4132073776132073777TC12GENIChomozygous112830814
4132073972132073973GA7GENIChomozygous112830815
4132074869132074870AG11GENIChomozygous112830817
4132075333132075334AT13GENIChomozygous113384093
4132075843132075844CT19GENIChomozygous113384095
4132076695132076696AT21GENIChomozygous112830820
4132078170132078171GA22GENIChomozygous113384097
4132083054132083055GC21GENIChomozygous112830825
4132085479132085480CT24GENIChomozygous113384103
4132086611132086612GA7GENIChomozygous113384106
4132087287132087288TC12GENIChomozygous112830842
4132088227132088228GA15GENIChomozygous113384108
4132088418132088419CT10GENIChomozygous113384110
4132091878132091879GA5GENICheterozygous113384112
4132093476132093477AG14GENIChomozygous112830850
4132094528132094529AG12GENIChomozygous112830851
4132094816132094817AG23GENIChomozygous112830852
4132095764132095765AG13GENIChomozygous113162689
4132099235132099236CT9GENIChomozygous113162691
4132099562132099563AG17GENIChomozygous113162693
4132101984132101985TA6GENIChomozygous113162697
4132102646132102647TG9GENIChomozygous113469707
4132103346132103347TC6GENIChomozygous113384116
4132104618132104619TG23GENIChomozygous113162699
4132105685132105686GA20GENIChomozygous113162701
4132106640132106641GA6GENIChomozygous113162702
4132106668132106669CT4GENIChomozygous126052939
4132107560132107561GA11GENIChomozygous113384118
4132109040132109041CT21GENICpossibly homozygous113162706