chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224854547224854548GA39GENIChomozygous57112597
4224854874224854875CG18GENIChomozygous57112600
4224854882224854883CT23GENIChomozygous57112602
4224856480224856481CT19GENIChomozygous57112604
4224856508224856509GGAAAAA16GENIChomozygous57112607
4224856682224856685CCT---1GENIChomozygous57112611
4224857816224857817CT27GENIChomozygous57112625
4224858318224858319TC28GENIChomozygous57112627
4224858530224858531AC30GENIChomozygous57112629
4224858803224858804AG9GENIChomozygous57112631
4224859155224859156CT45GENIChomozygous57112633
4224859484224859485CCAA23GENIChomozygous57112635
4224859712224859713AG18GENIChomozygous57112636
4224860556224860557CT26GENIChomozygous57112638
4224860679224860680TC19GENIChomozygous57112639
4224861526224861527TC24GENIChomozygous57112641
4224861563224861564CT25GENIChomozygous57112643
4224861932224861933AG23GENIChomozygous57112645
4224861996224861997TC17GENIChomozygous57112647
4224862039224862040GGTA12GENICheterozygous57112649
4224862369224862370TC16GENIChomozygous57112651
4224862844224862845GA25GENIChomozygous57112653
4224863155224863156GA27GENIChomozygous57112655
4224863771224863772TC25GENIChomozygous57112656
4224864670224864671GA22GENIChomozygous57112672
4224864907224864908GA23GENIChomozygous57112673
4224865416224865417CT11GENIChomozygous57112675
4224867581224867582CT20GENIChomozygous57112677
4224868401224868402TC23GENIChomozygous57112678
4224868413224868415CA--13GENICheterozygous58411305
4224868507224868508CT22GENIChomozygous57112680
4224871043224871044TG28GENIChomozygous57112682
4224871413224871414AG47GENIChomozygous57112684
4224872045224872073TGTGTGTGTGTGTGTGTGTGTGTGTGTA----------------------------21GENIChomozygous58663635
4224863933224863934CCTGACTGACTGAGTGACTGAG14GENICpossibly homozygous58376684
4224864180224864195TGTGTACGCGCGCGC---------------20GENICpossibly homozygous58376686
4224864195224864196GGA28GENIChomozygous58376688
4224873382224873386TCTG----13GENIChomozygous57112687