chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4182902235182902236GT49GENICpossibly homozygous57024811
4182902968182902969AATT5GENIChomozygous57024812
4182903165182903166AATT10GENIChomozygous57024813
4182903367182903368CCTT3GENIChomozygous57024814
4182903391182903392GGT10GENICpossibly homozygous57024815
4182903424182903425GT23GENICpossibly homozygous57024816
4182904338182904339GT55GENIChomozygous57024817
4182904878182904879TC53GENIChomozygous57024818
4182906158182906159TC40GENIChomozygous57024819
4182906352182906353TC48GENIChomozygous57024820
4182907213182907214A-1GENIChomozygous57024821
4182909156182909157AG43GENIChomozygous57024822
4182909240182909241A-25GENIChomozygous57024823
4182909260182909262TT--18GENICpossibly homozygous57024824
4182909261182909262T-18GENICheterozygous57024825
4182909506182909507GA8GENIChomozygous57024826
4182909510182909511GC6GENIChomozygous57024827
4182909511182909512GA6GENIChomozygous57024828
4182909515182909516AG7GENIChomozygous57024829
4182909519182909520GC8GENIChomozygous57024830
4182909527182909528TC8GENIChomozygous57024831
4182909529182909530GC8GENIChomozygous57024832
4182909553182909554G-7GENIChomozygous57024833
4182909560182909561AAT9GENIChomozygous57024834
4182909666182909667C-31GENIChomozygous57024835
4182909781182909782TC32GENIChomozygous57024836
4182909878182909879GA27GENICpossibly homozygous57024838
4182909957182909958TC13GENICheterozygous57559407