chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5163652471163652473TG--1GENIChomozygous56464006
5163652481163652484TGT---2GENIChomozygous56464007
5163652486163652487CCTTT2GENIChomozygous56464008
5163652544163652545GGC1GENIChomozygous56464009
5163653594163653598TGTG----3GENICheterozygous56570452
5163653596163653598TG--3GENICheterozygous56555063
5163653777163653778CG4GENIChomozygous56464010
5163657424163657425TC33GENIChomozygous55826957
5163658187163658188TC25GENIChomozygous55826959
5163658856163658857TC21GENIChomozygous55826961
5163659115163659116AATG25GENIChomozygous55826963
5163659133163659134TC24GENIChomozygous55826965
5163660463163660464CT28GENIChomozygous55826967
5163660656163660657AG30GENIChomozygous55826969
5163660932163660933CT34GENIChomozygous55826971
5163660933163660934CA34GENIChomozygous55826973
5163660952163660953AG38GENICpossibly homozygous55826975
5163661461163661462AC27GENIChomozygous55826977
5163661783163661784TTG10GENICheterozygous55826979
5163661783163661784TTGG10GENICpossibly homozygous55826981
5163662028163662032ATTC----7GENIChomozygous56464011
5163663523163663529TCCTCC------11GENIChomozygous55826985
5163663666163663681CTCCTCTTCTCCCTT---------------10GENIChomozygous56464012
5163664708163664709AC3GENIChomozygous55826997
5163664737163664738C-4GENIChomozygous55826999
5163665123163665124GT44GENIChomozygous55827001
5163665284163665285GA21GENIChomozygous55827003
5163665472163665473CT26GENIChomozygous55827005
5163666115163666116AC36GENIChomozygous55827007
5163666481163666482CA26GENIChomozygous55827009
5163666485163666486TA26GENIChomozygous55827011
5163666490163666491GA29GENIChomozygous55827013
5163666491163666492CT29GENIChomozygous55827015
5163666495163666496CT27GENIChomozygous55827017
5163666533163666534CT31GENIChomozygous55827019