chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4182902235182902236GT20GENIChomozygous57024811
4182903165182903166AATT16GENIChomozygous57024813
4182903391182903392GGT13GENIChomozygous57024815
4182903424182903425GT12GENIChomozygous57024816
4182904338182904339GT18GENIChomozygous57024817
4182904878182904879TC49GENIChomozygous57024818
4182906158182906159TC30GENIChomozygous57024819
4182906352182906353TC24GENIChomozygous57024820
4182907213182907214A-14GENICpossibly homozygous57024821
4182909156182909157AG29GENIChomozygous57024822
4182909240182909241A-26GENIChomozygous57024823
4182909260182909262TT--20GENIChomozygous57024824
4182909519182909520GC6GENIChomozygous57024830
4182909527182909528TC9GENIChomozygous57024831
4182909529182909530GC10GENIChomozygous57024832
4182909553182909554G-18GENIChomozygous57024833
4182909556182909557GA18GENIChomozygous58359724
4182909560182909561AAT18GENIChomozygous57024834
4182909666182909667C-40GENIChomozygous57024835
4182909667182909668CG42GENIChomozygous58298459
4182909781182909782TC30GENIChomozygous57024836
4182909858182909859T-22GENICpossibly homozygous57024837
4182909878182909879GA26GENIChomozygous57024838