chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5163653594163653598TGTG----11GENICheterozygous56570452
5163653596163653598TG--11GENICpossibly homozygous56555063
5163653777163653778CG12GENIChomozygous56464010
5163657424163657425TC27GENIChomozygous55826957
5163658187163658188TC20GENIChomozygous55826959
5163658856163658857TC19GENIChomozygous55826961
5163659115163659116AATG22GENIChomozygous55826963
5163659133163659134TC31GENIChomozygous55826965
5163660463163660464CT26GENIChomozygous55826967
5163660656163660657AG27GENIChomozygous55826969
5163660932163660933CT40GENIChomozygous55826971
5163660933163660934CA40GENIChomozygous55826973
5163660952163660953AG39GENIChomozygous55826975
5163661461163661462AC20GENIChomozygous55826977
5163661783163661784TTG3GENICheterozygous55826979
5163661783163661784TTGG3GENICheterozygous55826981
5163662028163662032ATTC----11GENIChomozygous56464011
5163663523163663529TCCTCC------10GENIChomozygous55826985
5163663666163663681CTCCTCTTCTCCCTT---------------17GENIChomozygous56464012
5163664737163664738C-2GENIChomozygous55826999
5163665123163665124GT14GENIChomozygous55827001
5163665284163665285GA23GENIChomozygous55827003
5163665472163665473CT15GENIChomozygous55827005
5163666115163666116AC19GENIChomozygous55827007
5163666481163666482CA21GENIChomozygous55827009
5163666485163666486TA21GENIChomozygous55827011
5163666490163666491GA24GENIChomozygous55827013
5163666491163666492CT24GENIChomozygous55827015
5163666495163666496CT23GENIChomozygous55827017
5163666533163666534CT20GENICpossibly homozygous55827019