chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83149982331499824GT23GENIChomozygous116446849
83150027831500279CT43GENIChomozygous116788762
83150220831502209CG37GENIChomozygous116788764
83150338631503387AG45GENIChomozygous116446854
83150343331503434TG39GENIChomozygous116446855
83150356631503567AG26GENIChomozygous116446856
83150376731503768CA30GENIChomozygous116446857
83150384631503847GT29GENIChomozygous116788766
83150401931504020GA24GENIChomozygous116446859
83150503431505035CT63GENIChomozygous116788768
83150567531505676AG38GENIChomozygous116446861
83150667331506674CT40GENIChomozygous116788770
83150840031508401TA17GENIChomozygous116446863
83151220031512201TC41GENIChomozygous116446866
83151468831514689GA16GENIChomozygous116446870
83151570631515707AG20GENIChomozygous116446873
83151780131517802TC26GENIChomozygous116446878
83151799531517996AG21GENIChomozygous116446879
83151817231518173TG18GENIChomozygous116788776
83151834231518343CT25GENIChomozygous116788778
83151955831519559AG26GENIChomozygous116788780
83151975231519753CT34GENIChomozygous116788782
83152693131526932TC28GENIChomozygous116446889
83152695031526951GA28GENIChomozygous116788790
83152744631527447AC35GENIChomozygous116446891
83152803331528034AG20GENIChomozygous116788792
83152822231528223TC23GENIChomozygous116446892
83152892831528929TC28GENIChomozygous116446893
83152997331529974AT39GENIChomozygous116446894
83153053831530539AG34GENIChomozygous116788794
83153197531531976TG25GENIChomozygous116446897
83153273631532737TC30GENIChomozygous116446899
83152640931526410TC28GENIChomozygous117909810