chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224854547224854548GA24GENIChomozygous57112597
4224854874224854875CG35GENIChomozygous57112600
4224854882224854883CT35GENIChomozygous57112602
4224856480224856481CT24GENIChomozygous57112604
4224856508224856509GGAAAAA19GENIChomozygous57112607
4224856682224856685CCT---1GENIChomozygous57112611
4224857816224857817CT34GENIChomozygous57112625
4224858318224858319TC24GENIChomozygous57112627
4224858530224858531AC35GENIChomozygous57112629
4224858803224858804AG32GENIChomozygous57112631
4224859155224859156CT13GENIChomozygous57112633
4224859484224859485CCAA20GENIChomozygous57112635
4224859712224859713AG35GENIChomozygous57112636
4224860556224860557CT46GENIChomozygous57112638
4224860679224860680TC35GENIChomozygous57112639
4224861526224861527TC21GENIChomozygous57112641
4224861563224861564CT28GENIChomozygous57112643
4224861932224861933AG18GENIChomozygous57112645
4224861996224861997TC16GENIChomozygous57112647
4224862369224862370TC25GENIChomozygous57112651
4224862844224862845GA23GENIChomozygous57112653
4224863155224863156GA32GENIChomozygous57112655
4224863771224863772TC12GENIChomozygous57112656
4224864670224864671GA37GENIChomozygous57112672
4224864907224864908GA44GENIChomozygous57112673
4224865416224865417CT36GENIChomozygous57112675
4224867581224867582CT35GENIChomozygous57112677
4224868401224868402TC20GENIChomozygous57112678
4224868412224868413GGCACA15GENICheterozygous57648756
4224868507224868508CT36GENIChomozygous57112680
4224871043224871044TG24GENIChomozygous57112682
4224871413224871414AG25GENIChomozygous57112684
4224868412224868413GGCA15GENICheterozygous58023888
4224863933224863934CCTGACTGACTGAGTGACTGAG24GENIChomozygous58376684
4224864180224864195TGTGTACGCGCGCGC---------------8GENICheterozygous58376686
4224864195224864196GGA9GENIChomozygous58376688
4224864178224864195TGTGTGTACGCGCGCGC-----------------8GENICheterozygous58411304
4224872065224872073TGTGTGTA--------1GENIChomozygous58376690
4224873382224873386TCTG----18GENIChomozygous57112687