chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81330646513306466CT26GENIChomozygous53090868
81330665813306659CT35GENIChomozygous53090869
81330699213306993TC33GENIChomozygous53090870
81330786213307866CACT----7GENICpossibly homozygous53090871
81330788213307883TC18GENICheterozygous53180540
81330798613307987AACCAT12GENICpossibly homozygous53090872
81330804913308053CCAT----19GENICheterozygous53090873
81330806613308067CT28GENICheterozygous53247304
81330813513308136TC20GENICheterozygous53180541
81330815813308159GA14GENICheterozygous53090874
81330815913308160CT15GENICheterozygous53090875
81330815913308160CCCCAT9GENIChomozygous53090876
81330912613309127TC41GENIChomozygous53090877
81330913913309140GA45GENIChomozygous53090878
81330993313309935CA--14GENICheterozygous53090879
81331108513311086GA17GENIChomozygous53090880
81331129513311296CT19GENIChomozygous53090881
81331165513311656AG26GENIChomozygous53090882
81331226813312269TG19GENIChomozygous53090883
81331227213312273TC19GENIChomozygous53090884
81331240113312421CTTGGAACTTCTAGGAGGCA--------------------4GENIChomozygous53090885
81331245413312455GA15GENIChomozygous53090886
81331295613312957TC24GENIChomozygous53090887
81331329113313292AACACT29GENIChomozygous53090888
81331347213313473GC25GENIChomozygous53090889
81331372113313722GA28GENIChomozygous53090890
81331412213314123TC27GENIChomozygous53090891
81331439813314399CT27GENIChomozygous53090892
81331511613315117CT14GENIChomozygous53090893
81331544613315451GGAGG-----12GENIChomozygous53090894
81331577213315773TA19GENIChomozygous53090895
81331582413315825TA23GENIChomozygous53090896
81331590913315910TC15GENIChomozygous53090897
81331624513316246A-15GENIChomozygous53090898