chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83149982331499824GT29GENIChomozygous116446849
83150003031500031TC31GENIChomozygous116446851
83150146031501461CT26GENIChomozygous118058629
83150220831502209CG29GENIChomozygous116788764
83150338631503387AG35GENIChomozygous116446854
83150343331503434TG37GENIChomozygous116446855
83150356631503567AG32GENIChomozygous116446856
83150376731503768CA34GENIChomozygous116446857
83150384631503847GT36GENIChomozygous116788766
83150401931504020GA41GENIChomozygous116446859
83150567531505676AG31GENIChomozygous116446861
83150667331506674CT37GENIChomozygous116788770
83151182931511830TG41GENIChomozygous116446864
83151204931512050AT43GENIChomozygous116446865
83151220031512201TC42GENIChomozygous116446866
83151234631512347CT37GENIChomozygous116446867
83151318931513190GT23GENIChomozygous118058630
83151374931513750CA39GENIChomozygous116446868
83151464931514650GA26GENIChomozygous116446869
83151468831514689GA18GENIChomozygous116446870
83151544531515446GA39GENIChomozygous116446872
83151570631515707AG22GENIChomozygous116446873
83151840631518407GA29GENIChomozygous116446880
83151780131517802TC35GENIChomozygous116446878
83151799531517996AG35GENIChomozygous116446879
83151897231518973CT31GENIChomozygous116446881
83151898531518986TG30GENIChomozygous116446882
83152693131526932TC52GENIChomozygous116446889
83152695031526951GA47GENIChomozygous116788790
83152744631527447AC29GENIChomozygous116446891
83152803331528034AG39GENIChomozygous116788792
83152822231528223TC34GENIChomozygous116446892
83152892831528929TC31GENIChomozygous116446893
83152923731529238GA31GENIChomozygous117915802
83152997331529974AT47GENIChomozygous116446894
83153197531531976TG35GENIChomozygous116446897
83153273631532737TC34GENIChomozygous116446899
83153304531533046CT46GENIChomozygous117960834
83152640931526410TC47GENIChomozygous117909810