chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173871116138711162CT52GENIChomozygous111041029
173871147938711480TG66GENIChomozygous111041031
173871162238711623GT92GENIChomozygous111041033
173871244638712447GT50GENIChomozygous111041035
173871304638713047TC37GENIChomozygous111199967
173871323838713239TA85GENIChomozygous111041037
173871356138713562CT75GENIChomozygous111041039
173871385238713853AG54GENIChomozygous111041041
173871405438714055GA32GENIChomozygous111041043
173871421638714217CT68GENIChomozygous111199973
173871454938714550TC61GENIChomozygous111199975
173871461138714612AG72GENIChomozygous111041045
173871558438715585AG68GENICpossibly homozygous111041047