chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3171277985171277986CA21GENIChomozygous112206107
3171278058171278059TA30GENIChomozygous112206109
3171278427171278428AG38GENIChomozygous112206111
3171278611171278612CT29GENIChomozygous112206113
3171279421171279422CT26GENIChomozygous112206115
3171279664171279665GA26GENIChomozygous112206117
3171280493171280494AC31GENICpossibly homozygous112206119
3171282590171282591GA21GENIChomozygous112206121
3171284163171284164GT33GENIChomozygous119686545
3171284165171284166GT34GENIChomozygous119686546
3171287746171287747TC21GENIChomozygous112206123
3171288625171288626TC26GENIChomozygous112206125
3171290841171290842AT30GENIChomozygous112206127