chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1231845942231845943AC36GENIChomozygous584743719
1231847735231847736AG38GENIChomozygous584743720
1231849198231849199T-32GENIChomozygous718046559
1231849363231849364CT14GENIChomozygous584743721
1231849975231849976AG28GENIChomozygous584743722
1231850297231850298TA47GENIChomozygous584743723
1231850316231850317TC39GENIChomozygous584743724
1231851532231851533AT47GENIChomozygous584743725
1231853003231853004TTA20GENICpossibly homozygous718046562
1231853003231853004TTAAA20GENICheterozygous718046563
1231853294231853295G-34GENIChomozygous718046564
1231853480231853481TTA20GENIChomozygous718046565
1231854937231854938GA56GENIChomozygous584743726
1231856251231856252TTACACACACAC3GENIChomozygous718046568
1231856338231856339CCA30GENIChomozygous718046569
1231856456231856458CA--22GENICheterozygous718046570
1231857022231857023GA33GENIChomozygous584743727
1231857163231857164CA35GENIChomozygous584743728
1231857946231857947CCA28GENICpossibly homozygous718046571
1231857960231857961TG35GENIChomozygous584743729