chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81330646513306466CT38GENIChomozygous53090868
81330665813306659CT40GENIChomozygous53090869
81330699213306993TC18GENIChomozygous53090870
81330786213307866CACT----10GENIChomozygous53090871
81330788213307883TC29GENICheterozygous53180540
81330798613307987AACCAT9GENICpossibly homozygous53090872
81330804913308053CCAT----7GENICpossibly homozygous53090873
81330813513308136TC21GENICheterozygous53180541
81330815813308159GA28GENICheterozygous53090874
81330815913308160CT29GENICheterozygous53090875
81330815913308160CCCCAT13GENICheterozygous53090876
81330912613309127TC36GENIChomozygous53090877
81330913913309140GA40GENIChomozygous53090878
81330993313309935CA--17GENICheterozygous53090879
81331108513311086GA21GENIChomozygous53090880
81331129513311296CT29GENIChomozygous53090881
81331165513311656AG23GENIChomozygous53090882
81331226813312269TG25GENIChomozygous53090883
81331227213312273TC24GENIChomozygous53090884
81331240113312421CTTGGAACTTCTAGGAGGCA--------------------4GENIChomozygous53090885
81331245413312455GA24GENIChomozygous53090886
81331295613312957TC36GENIChomozygous53090887
81331329113313292AACACT18GENIChomozygous53090888
81331347213313473GC24GENIChomozygous53090889
81331372113313722GA29GENIChomozygous53090890
81331412213314123TC33GENIChomozygous53090891
81331439813314399CT31GENIChomozygous53090892
81331511613315117CT19GENIChomozygous53090893
81331544613315451GGAGG-----17GENIChomozygous53090894
81331545513315456GA22GENICheterozygous53180542
81331577213315773TA23GENIChomozygous53090895
81331582413315825TA17GENIChomozygous53090896
81331590913315910TC38GENIChomozygous53090897
81331624513316246A-13GENICpossibly homozygous53090898