chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103755680037556801GA36GENIChomozygous51417882
103755731337557314TTAA16GENICheterozygous51417884
103755731337557314TTA16GENICheterozygous51417886
103755733337557334CT31GENIChomozygous51417888
103755783037557831CT24GENIChomozygous51417890
103755849137558492AT31GENIChomozygous51417892
103755865637558657GA38GENIChomozygous51417894
103755867237558673CT35GENIChomozygous51417896
103755868337558684GA38GENIChomozygous51417898
103755870637558707TG36GENIChomozygous51417900
103755946937559489ACAGTCACACACAGTCACAT--------------------15GENICpossibly homozygous51417902
103755953537559537AC--14GENICpossibly homozygous51417904
103755956237559563TG13GENIChomozygous51417906
103755962037559621C-11GENICheterozygous51417908
103755962037559621CCA10GENICheterozygous51417910
103756015237560153CT33GENIChomozygous51417918
103756028037560285TGGTG-----17GENIChomozygous51417920
103756031337560314CT23GENIChomozygous51417922
103756036137560362TG33GENIChomozygous51417924
103756095337560954GA31GENIChomozygous51417926
103756166137561662TA40GENIChomozygous51417928
103756174837561749TC42GENIChomozygous51417930
103756197037561971TC30GENIChomozygous51417932
103756223337562234GC43GENIChomozygous51417934
103756284137562842GA23GENIChomozygous52140204
103756056137560562CT36GENIChomozygous52140196
103756122337561224GT37GENIChomozygous52140198
103756122437561225GT37GENIChomozygous52140200
103756156137561562AACTC24GENIChomozygous52140202
103756423437564235GGT24GENIChomozygous51417936
103756531137565315AAAA----3GENIChomozygous51417938
103756577037565771CCGT31GENICpossibly homozygous51417940
103756626437566266CC--2GENIChomozygous51849828
103756645837566459TTG13GENICheterozygous51417942
103756645837566459TTGG13GENICpossibly homozygous51634522
103756766137567666TTTTT-----8GENIChomozygous52140206