chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224854547224854548GA19GENIChomozygous57112597
4224854874224854875CG18GENIChomozygous57112600
4224854882224854883CT18GENIChomozygous57112602
4224856480224856481CT8GENIChomozygous57112604
4224856508224856509GGAAAAA6GENIChomozygous57112607
4224856682224856685CCT---8GENIChomozygous57112611
4224857816224857817CT24GENIChomozygous57112625
4224858318224858319TC26GENIChomozygous57112627
4224858530224858531AC21GENIChomozygous57112629
4224858803224858804AG25GENIChomozygous57112631
4224859155224859156CT23GENIChomozygous57112633
4224859484224859485CCAA52GENIChomozygous57112635
4224859712224859713AG34GENIChomozygous57112636
4224860556224860557CT37GENIChomozygous57112638
4224860679224860680TC29GENIChomozygous57112639
4224861526224861527TC28GENIChomozygous57112641
4224861563224861564CT23GENIChomozygous57112643
4224861932224861933AG14GENIChomozygous57112645
4224861996224861997TC19GENIChomozygous57112647
4224862039224862040GGTA20GENICpossibly homozygous57112649
4224862369224862370TC17GENIChomozygous57112651
4224862844224862845GA25GENIChomozygous57112653
4224863155224863156GA28GENIChomozygous57112655
4224863771224863772TC14GENIChomozygous57112656
4224864670224864671GA15GENIChomozygous57112672
4224864907224864908GA30GENIChomozygous57112673
4224865416224865417CT22GENIChomozygous57112675
4224867581224867582CT27GENIChomozygous57112677
4224868401224868402TC26GENIChomozygous57112678
4224863933224863934CCTGACTGACTGAGTGACTGAG4GENIChomozygous58376684
4224864180224864195TGTGTACGCGCGCGC---------------8GENIChomozygous58376686
4224864195224864196GGA11GENIChomozygous58376688
4224868413224868415CA--10GENICheterozygous58411305
4224868507224868508CT25GENIChomozygous57112680
4224871043224871044TG21GENIChomozygous57112682
4224871413224871414AG18GENIChomozygous57112684
4224873382224873386TCTG----9GENIChomozygous57112687
4224872045224872073TGTGTGTGTGTGTGTGTGTGTGTGTGTA----------------------------14GENIChomozygous58663635