chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5163653648163653649G-2GENICheterozygous55826935
5163653666163653668TA--3GENICheterozygous55826937
5163654125163654126TTG13GENICheterozygous55826943
5163654833163654838AAAAA-----6GENICheterozygous56192892
5163654834163654838AAAA----6GENICheterozygous55826945
5163654916163654917T-14GENICheterozygous55826947
5163655102163655103TG12GENICheterozygous55826949
5163655111163655112AT11GENICheterozygous55826951
5163657424163657425TC31GENICpossibly homozygous55826957
5163658187163658188TC33GENIChomozygous55826959
5163658856163658857TC16GENIChomozygous55826961
5163659115163659116AATG31GENIChomozygous55826963
5163659133163659134TC33GENIChomozygous55826965
5163660463163660464CT22GENIChomozygous55826967
5163660656163660657AG36GENIChomozygous55826969
5163660932163660933CT26GENIChomozygous55826971
5163660933163660934CA26GENIChomozygous55826973
5163660952163660953AG20GENIChomozygous55826975
5163661461163661462AC22GENIChomozygous55826977
5163661783163661784TTG8GENICheterozygous55826979
5163661783163661784TTGG8GENICpossibly homozygous55826981
5163662032163662034AT--10GENIChomozygous55826983
5163663523163663529TCCTCC------9GENICheterozygous55826985
5163663535163663536TC12GENICheterozygous55826987
5163663655163663656T-10GENICheterozygous55826989
5163663680163663681TC13GENICpossibly homozygous55826995
5163664708163664709AC4GENIChomozygous55826997
5163664737163664738C-2GENIChomozygous55826999
5163665123163665124GT23GENIChomozygous55827001
5163665284163665285GA27GENIChomozygous55827003
5163665472163665473CT33GENIChomozygous55827005
5163666115163666116AC22GENIChomozygous55827007
5163666481163666482CA20GENIChomozygous55827009
5163666485163666486TA20GENIChomozygous55827011
5163666490163666491GA19GENIChomozygous55827013
5163666491163666492CT20GENIChomozygous55827015
5163666495163666496CT20GENIChomozygous55827017
5163666533163666534CT21GENIChomozygous55827019