chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
19017837090178371GA26GENIChomozygous606529502
19017892590178926AG19GENIChomozygous606529503
19017991190179912GGA12GENICheterozygous731704137
19017991290179913A-12GENICheterozygous731704136
19018039890180399AG12GENIChomozygous608831418
19018190490181905AAT18GENICheterozygous731704139
19018190490181905AATT18GENICpossibly homozygous731704140
19018190490181905AATTT18GENICheterozygous731704141
19018445890184459TA23GENIChomozygous606529504
19018477490184775GC13GENIChomozygous606529505
19018479590184796AAAG7GENIChomozygous731704144
19018758390187585CT--10GENIChomozygous731704148
19019042190190422TTA11GENICheterozygous731704150
19019042190190422TTAA11GENICheterozygous731704151
19019186690191867TTA9GENICheterozygous731704153
19019186790191868A-9GENICheterozygous731704152
19019620390196204GGCACTGGT28GENIChomozygous731704154
19019620590196206AAAAC28GENIChomozygous731704155