chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
192507970925079710CT41GENIChomozygous109866748
192508006925080070GA55GENIChomozygous109866750
192508193025081931AG54GENICpossibly homozygous109866752
192508194825081949AG59GENICpossibly homozygous109672176
192508211825082119AG24GENIChomozygous119602462
192508287425082875CT60GENIChomozygous109866754
192508465325084654GT43GENIChomozygous109866758
192508224325082244GA37GENIChomozygous124557776
192508581425085815G33GENIChomozygous129595726
192508581725085818T33GENIChomozygous129595727
192508582125085821GCCGT35GENIChomozygous129595728
192508582425085824CA34GENIChomozygous129595729
192508582525085839TTCTGTGTTGTTTT32GENIChomozygous129595730
192508584325085843CT33GENIChomozygous129595731
192508584725085848TA29GENIChomozygous124557784
192508584925085849CC29GENIChomozygous129595732
192508585225085853CG29GENIChomozygous124557786
192508585325085854GA29GENIChomozygous124557787
192508586125085862TA29GENIChomozygous124557788
192508586225085863AT29GENIChomozygous124557789
192508588025085880GT22GENIChomozygous129595733
192508588525085886G18GENIChomozygous129595734
192508589025085890C18GENIChomozygous129595735
192508589825085898GG17GENIChomozygous129595736
192508590225085902CCAAA17GENIChomozygous129595737
192508590525085913CTTGGTCG17GENIChomozygous129595738
192508591625085918TC17GENIChomozygous129595739
192508592025085921A17GENIChomozygous129595740
192508592825085928TA17GENIChomozygous129595741
192508841125088412GC44GENIChomozygous109672180
192508974925089750TC55GENIChomozygous109672184
192508984625089847CG60GENIChomozygous109866760
192509033925090340CT62GENIChomozygous109866762
192509107725091078CA27GENICpossibly homozygous109866768
192509138625091387G48GENIChomozygous129595742
192509139625091397C43GENIChomozygous129595743
192509140625091407A46GENIChomozygous129595744
192508949025089491C27GENIChomozygous134464797
192509138125091382GC50GENIChomozygous109672188
192509140325091404GC45GENIChomozygous109672190
192509141125091412AT47GENIChomozygous109672192