chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171191107811911079TTAGGGGTGTGC1GENIChomozygous47898734
171191396211913963CG19GENICpossibly homozygous47021263
171191414711914148TA22GENIChomozygous47021264
171191445211914453CT18GENICheterozygous47021265
171191938011919381TG29GENICpossibly homozygous47021270
171192133411921335TC16GENICpossibly homozygous47021271
171192164811921649TC18GENIChomozygous47021272
171192238911922390AG15GENIChomozygous47021273
171192247211922473CCA12GENIChomozygous47021274
171192353011923531GA23GENICpossibly homozygous47021275
171192367711923678GA13GENICheterozygous47021276
171192399111923992GA22GENICpossibly homozygous47021277