chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104530960445309605A-14GENICpossibly homozygous51442195
104530962845309629AAAC20GENICpossibly homozygous52372916
104531021845310219GGTT13GENICheterozygous52372919
104531021845310219GGTTT13GENICheterozygous52372921
104531148945311490AACTCCCCAAT23GENIChomozygous51442198
104531169245311693GA27GENIChomozygous51442199