chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72637963026379631TG19GENIChomozygous115624148
72638570726385708CA9GENIChomozygous115624158
72638869226388693AG14GENIChomozygous115624161
72638882326388824TG17GENIChomozygous115624162
72638887926388880GC16GENIChomozygous115624163
72639368226393683GA19GENICheterozygous115624176
72640198226401983GT16GENICpossibly homozygous115624189
72640211426402115GT8GENIChomozygous115624190
72640212126402122GT9GENIChomozygous115624191
72640213726402138GT10GENIChomozygous115624192
72640214126402142GT10GENIChomozygous115624193
72640977926409780CT19GENIChomozygous115624216
72640982226409823GA16GENIChomozygous115624217
72640982626409827CA14GENIChomozygous115624218
72641038026410381GC10GENIChomozygous115624219
72641057826410579AT14GENIChomozygous115624220