chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161912696019126961CT35GENIChomozygous139889652
161912703719127038AC41GENIChomozygous145884861
161912770819127709GA33GENIChomozygous145884862
161912791419127915CT28GENIChomozygous139889653
161912809119128091AG28GENICpossibly homozygous145880869
161912873019128731TG35GENIChomozygous139889655
161912911919129120GC33GENIChomozygous139889656
161912951319129514AG34GENIChomozygous139889657
161912993219129933CT27GENIChomozygous145884863
161913047119130472AG23GENIChomozygous139889658