chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119701430119701431AG2GENIChomozygous54082051
7119701440119701441GA3GENICheterozygous54082052
7119701543119701544CT14GENICpossibly homozygous54082053
7119701611119701612AG13GENIChomozygous54082054
7119701981119701982GA12GENICpossibly homozygous54673137
7119702691119702692GGGAGCCCGGAAGGCAACT3GENICheterozygous54082060
7119702748119702749TC17GENIChomozygous54082062
7119703416119703417AG10GENIChomozygous54082063
7119703694119703695C-12GENIChomozygous54673139
7119704024119704025AG4GENIChomozygous54673141
7119704037119704038GC7GENICpossibly homozygous54673143
7119704409119704410TC20GENICpossibly homozygous54673145
7119704977119704978AG6GENIChomozygous54673147
7119705272119705273TC14GENIChomozygous54082064
7119706360119706361AG23INTERGENICpossibly homozygous54082065
7119706543119706544AC19INTERGENICheterozygous54082067
7119707003119707004TC13INTERGENICpossibly homozygous54082068
7119707575119707576A-14INTERGENICpossibly homozygous54673152
7119708675119708676GA16INTERGENICpossibly homozygous54082071
7119708829119708830GA24INTERGENIChomozygous54673154
7119709484119709485AAG5INTERGENIChomozygous54673156
7119709609119709610GA8INTERGENICpossibly homozygous54673158
7119713778119713779GA15INTERGENIChomozygous54673160
7119716047119716048AG20INTERGENICpossibly homozygous54082078