chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14100167624100167625GA22GENIChomozygous49239120
14100167691100167693TC--3GENIChomozygous49319120
14100167693100167694CG3GENIChomozygous49319121
14100168495100168496GA36GENIChomozygous49239122
14100168581100168582CT37GENIChomozygous49239123
14100168743100168744GA30GENIChomozygous49252605
14100168906100168907GGGGGAA8GENIChomozygous49239125
14100169516100169551AGTTAAGCCCGCCTGATGGCTTGTCTTTGTTCTCA-----------------------------------31GENIChomozygous49319122
14100169813100169814GA26GENIChomozygous49239132
14100170495100170496CCT10GENICpossibly homozygous49186200
14100170569100170570GT24GENIChomozygous49239133
14100170588100170589GA24GENIChomozygous49239135
14100170794100170795GA30GENIChomozygous49239136
14100171093100171094GA40GENIChomozygous49252606
14100171522100171524CT--28GENIChomozygous49239138
14100171898100171899TG38GENIChomozygous49239140
14100172053100172054CT32GENIChomozygous49239142
14100172093100172094CT35GENIChomozygous49239144
14100172770100172771AG24GENIChomozygous49239147
14100173348100173349AG37GENIChomozygous49239149
14100173719100173720GT31GENIChomozygous49239151
14100173808100173809CT36GENIChomozygous49252607
14100173847100173848CT36GENIChomozygous49239153
14100173997100173998TC20GENIChomozygous49239155
14100174208100174209TC23GENIChomozygous49239156
14100174418100174419CT36GENIChomozygous48858473
14100174850100174851CT19GENIChomozygous49252608
14100175072100175073TC23GENIChomozygous49239158