chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101341173313411734CT31GENIChomozygous116495984
101341183313411834GA31GENIChomozygous116495986
101341352713413528CA29GENIChomozygous116495990
101341377113413772AG38GENIChomozygous116495994
101341400713414008AT31GENIChomozygous116495998
101341402113414022GA26GENIChomozygous116496000
101341404813414049TC33GENIChomozygous116496002
101341406113414062CT34GENIChomozygous116496004
101341410313414104TC44GENIChomozygous116496008
101341538213415383GA38GENIChomozygous116496010
101341581213415813AG29GENIChomozygous116496012
101341606213416063GA17GENIChomozygous116496014
101341745113417452GA36GENIChomozygous116496016
101341821913418220TC14GENIChomozygous117120342