chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123766874937668750AG8GENIChomozygous115321201
123766875137668752AG8GENIChomozygous115321203
123766880137668801G16GENIChomozygous128986165
123766882437668825T18GENIChomozygous128986166
123766884137668841C18GENIChomozygous128986167
123766884637668846C17GENIChomozygous128986168
123766885637668856C16GENIChomozygous128986169
123766886937668869C14GENIChomozygous128986170
123766891137668912T18GENIChomozygous128986171
123766891637668917A18GENIChomozygous128986172
123766892037668921G19GENIChomozygous128986173
123766898837668990GT16GENIChomozygous128986178
123766892637668927C19GENIChomozygous128986174
123766893937668940G16GENIChomozygous128986175
123766895137668952A13GENIChomozygous128986176
123766896837668968GG12GENIChomozygous128986177
123766885037668851GC18GENIChomozygous115525352
123766899837668998G18GENIChomozygous128986179
123766904537669046TC14GENIChomozygous115321205
123767174937671750TC25GENIChomozygous115321207
123766952637669527GA40GENIChomozygous115440073
123767079137670792TC43GENIChomozygous115440074
123767153037671531TC40GENIChomozygous115440075
123766958437669585TA33GENIChomozygous115381207
123767027337670274G49GENIChomozygous131493247
123767139137671392C60GENIChomozygous131493248
123767299437672995CG51GENIChomozygous115321209
123767349937673500TC33GENIChomozygous115321211
123767390537673906AG39GENIChomozygous115381213
123767392437673925TC40GENIChomozygous115321213
123767401937674020CT40GENIChomozygous115440076
123767425537674256TC46GENICheterozygous115525354
123767453737674538CT44GENIChomozygous115381217
123767660137676602AT77GENICheterozygous115525356
123767272237672723CT43GENICpossibly homozygous115608791
123767492337674926TAT34GENIChomozygous132705923