chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224854547224854548GA15GENICpossibly homozygous57112597
4224854874224854875CG3GENIChomozygous57112600
4224854882224854883CT4GENICheterozygous57112602
4224857816224857817CT8GENICheterozygous57112625
4224858530224858531AC10GENIChomozygous57112629
4224858803224858804AG21GENIChomozygous57112631
4224859155224859156CT13GENIChomozygous57112633
4224859484224859485CCAA1GENIChomozygous57112635
4224859712224859713AG25GENIChomozygous57112636
4224860556224860557CT22GENIChomozygous57112638
4224860679224860680TC18GENICpossibly homozygous57112639
4224861526224861527TC12GENIChomozygous57112641
4224861563224861564CT9GENICpossibly homozygous57112643
4224861932224861933AG1GENIChomozygous57112645
4224862369224862370TC14GENICpossibly homozygous57112651
4224862844224862845GA24GENIChomozygous57112653
4224863155224863156GA16GENICpossibly homozygous57112655
4224863771224863772TC1GENIChomozygous57112656
4224864670224864671GA13GENICpossibly homozygous57112672
4224864907224864908GA6GENIChomozygous57112673
4224865416224865417CT24GENICpossibly homozygous57112675
4224871043224871044TG14GENIChomozygous57112682
4224867581224867582CT24GENIChomozygous57112677
4224868401224868402TC18GENICpossibly homozygous57112678
4224868507224868508CT11GENIChomozygous57112680
4224871413224871414AG17GENIChomozygous57112684
4224871987224871988A-2GENIChomozygous58023890