chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36269513362695134TC7GENIChomozygous57400804
36269522062695221AG16GENICpossibly homozygous57400805
36269542762695428CA20GENIChomozygous57400806
36269567162695672CT6GENIChomozygous57400807
36269567462695675GA5GENIChomozygous57400808
36269568662695687CT7GENIChomozygous57400809
36269594862695949GA12GENIChomozygous57400810
36269749862697499GGT17GENIChomozygous57400811
36269768862697689CG27GENICpossibly homozygous57400812
36269816162698162TC6GENICheterozygous57400813
36269816562698168TTG---4GENICheterozygous57400814
36269932262699323CG24GENIChomozygous57400816
36269954962699550GA8GENIChomozygous57400817
36270027262700273AG9GENIChomozygous57400818
36270074162700742GA5GENIChomozygous57891661
36270084962700850CT8GENIChomozygous57400820
36270092962700930GA10GENICpossibly homozygous57400821
36270233362702334TC18GENIChomozygous57400822
36270325862703259GA16GENIChomozygous57400823
36270375062703751TTA14GENIChomozygous57400824
36270405762704058AG20GENIChomozygous57400825
36270429762704298TC12GENICheterozygous57400826
36270447962704480GA12GENICheterozygous57400827
36270496562704966TC10GENICpossibly homozygous57400829
36270548762705488GA4GENIChomozygous57400830
36270561362705614GT9GENIChomozygous57400831