chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1218481172218481173CA30GENIChomozygous108538284
1218482114218482115TC26GENIChomozygous108538285
1218484419218484420AG5GENIChomozygous108538288
1218484796218484797CT12GENIChomozygous108538289
1218486498218486499GA17GENIChomozygous108538290
1218486616218486617AC8GENIChomozygous120475918
1218486683218486684GA21GENICpossibly homozygous108538291
1218487988218487989GT19GENIChomozygous108538293
1218491188218491189TC15GENIChomozygous108538294
1218491505218491506TC8GENIChomozygous108538295
1218491583218491584GA16GENIChomozygous108538296
1218491679218491680TA16GENIChomozygous108538297
1218491892218491893TC17GENIChomozygous108538298
1218491904218491905TC18GENIChomozygous108538299