chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
157535328775353288CCA47GENIChomozygous691419511
157535329175353292TA50GENIChomozygous523126407
157535353275353533CT50GENIChomozygous520501367
157535388275353883AG43GENIChomozygous520501368
157535405675354057CT41GENIChomozygous520501369
157535448875354489GC58GENIChomozygous520501370
157535477975354780GA61GENICpossibly homozygous520501371
157535682075356821AG32GENIChomozygous520501372
157535686075356861AG34GENIChomozygous520501373
157535842675358427TTG21GENIChomozygous691419512
157535865975358660GT43GENIChomozygous520501374
157535890875358909AC35GENIChomozygous520501375
157535917475359175TC38GENIChomozygous520501376
157535926475359265GA28GENIChomozygous520501377