chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15731888457318884T38GENICpossibly homozygous127385991
15731949857319499TC58GENIChomozygous108111387
15732055357320554AG57GENIChomozygous108111388
15732375957323760GA52GENIChomozygous108111389
15732448457324485CT56GENIChomozygous108111390
15732533657325336TC38GENIChomozygous127385992
15732661957326620CA74GENIChomozygous108111391
15732338057323381AC15GENICheterozygous130623981