chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108907912489079125CT47GENIChomozygous116675040
108907956589079566AG48GENIChomozygous116675042
108907981689079817TC46GENIChomozygous116675044
108907988189079882CT50GENIChomozygous116675046
108907989489079895CT46GENIChomozygous116902166
108908292289082923CT49GENIChomozygous116675048
108908341389083414CT40GENIChomozygous116675050
108908481189084812GA34GENICpossibly homozygous116675052