chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173871116138711162CT30GENIChomozygous111041029
173871147938711480TG26GENICpossibly homozygous111041031
173871356138713562CT33GENIChomozygous111041039
173871162238711623GT29GENIChomozygous111041033
173871244638712447GT18GENIChomozygous111041035
173871323838713239TA30GENIChomozygous111041037
173871304638713047TC22GENIChomozygous111199967
173871385238713853AG17GENIChomozygous111041041
173871405438714055GA22GENIChomozygous111041043
173871421638714217CT21GENIChomozygous111199973
173871454938714550TC30GENIChomozygous111199975
173871461138714612AG20GENIChomozygous111041045
173871558438715585AG30GENIChomozygous111041047