chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125746090125746091CT22GENIChomozygous652860632
7125747342125747343CT16GENIChomozygous652860633
7125747534125747535CT12GENIChomozygous652860634
7125747571125747572GA24GENIChomozygous652860635
7125748329125748330AG25GENIChomozygous652860636
7125748832125748833C-3GENIChomozygous758742028
7125748927125748928GA20GENIChomozygous652860637
7125749012125749013GA16GENIChomozygous652860638
7125749414125749415AG22GENIChomozygous652860639
7125751521125751522AATT9GENICpossibly homozygous758742030
7125752000125752001TC23GENIChomozygous652860640
7125752756125752757GA17GENIChomozygous652860641
7125753821125753822CT9GENICpossibly homozygous652860642
7125753897125753898CT17GENIChomozygous652860643
7125753949125753950GA21GENIChomozygous652860644
7125754274125754275AG19GENIChomozygous652860645
7125754320125754321CT25GENIChomozygous652860646
7125754367125754368CT22GENIChomozygous652860647
7125754379125754380GC20GENIChomozygous652860648
7125755157125755158GA13GENIChomozygous652860649
7125755666125755667CT16GENIChomozygous652860650
7125755703125755704CT14GENIChomozygous652860651
7125756500125756501TC22GENIChomozygous652860652
7125756849125756850AG11GENIChomozygous652860653
7125756965125756966GGAAAA8GENICheterozygous758742032
7125756965125756966GGAAAAAAAAAAA8GENICheterozygous758742033
7125757153125757154TTA7GENIChomozygous758742034