chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
462977726297773CT14GENIChomozygous112478689
462985716298572TC13GENIChomozygous112478691
462989896298990GA21GENIChomozygous112478693
463001016300102TG22GENIChomozygous113433019
463006546300655TC14GENIChomozygous112478695
463006596300660AG15GENIChomozygous112478697
463008486300849AG15GENIChomozygous112478699
463009456300946AG12GENIChomozygous112478701
463013476301348CG18GENIChomozygous112478703
463019186301919AG24GENIChomozygous112478705
463023596302360T13GENIChomozygous128001862
463045436304544GA15GENIChomozygous113433021
463048686304869TC14GENIChomozygous112478711
463049156304916TA15GENIChomozygous112478715
463060346306037AGA22GENIChomozygous128001863
463086066308607CA19GENIChomozygous113433023
463026486302652TGGT25GENIChomozygous130925265
463088766308876AAAC3GENIChomozygous130925266
463044176304417C9GENIChomozygous130293210
463054686305469GA23GENIChomozygous112478717
463066326306633TA15GENIChomozygous112478719
463067006306701AG23GENIChomozygous112478721
463072676307268CT22GENIChomozygous112478723
463077386307739TG23GENIChomozygous112478727
463154026315403TC18GENIChomozygous112478731
463161106316111AT27GENIChomozygous112478733
463162086316209TC21GENIChomozygous112478735
463170976317098TC19GENIChomozygous112478741
463179096317910CT23GENIChomozygous113433025
463218976321897TTC13GENIChomozygous128001870
463229176322918CT20GENIChomozygous112478745
463251366325137AG15GENIChomozygous112478746
463273966327397TC10GENICpossibly homozygous112478754
463257436325744GA16GENIChomozygous112478748
463260126326013AG9GENIChomozygous112478750
463260856326086CT11GENIChomozygous112478752
463290766329077GA11GENIChomozygous112478756
463299706329971TC14GENIChomozygous112478760
463301786330179GA15GENIChomozygous112478762
463303826330383TC12GENIChomozygous113433027
463304666330467GA12GENIChomozygous112478764