chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153706789837067899AG16GENICpossibly homozygous48501096
153707019537070196TC23GENIChomozygous48501098
153707298737072988CCTGA12GENIChomozygous48501100
153707356137073562TTG19GENIChomozygous48501104
153707488237074883AC14GENICpossibly homozygous48501106
153707512237075123TC15GENICpossibly homozygous48501108
153707702037077021GA12GENIChomozygous48501112
153707728437077285GA10GENIChomozygous48501114
153707767637077677AT13GENICheterozygous48501116