chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2240467983240467984CT52GENIChomozygous110334098
2240470124240470125CT55GENIChomozygous110334099
2240470450240470451AG47GENIChomozygous110334102
2240471400240471401CA51GENIChomozygous110334104
2240471579240471580TC41GENIChomozygous110334106
2240471735240471736CA25GENIChomozygous110334108
2240472260240472261TC26GENIChomozygous110334110
2240472376240472377AC49GENIChomozygous110334111
2240472811240472812GC56GENIChomozygous110334113
2240473575240473576GA64GENIChomozygous110334115
2240473628240473629GA55GENIChomozygous110334117
2240473762240473763AG55GENIChomozygous110334119
2240473903240473904AG40GENIChomozygous110334121
2240475341240475342GA41GENIChomozygous110334123
2240475780240475781AG47GENIChomozygous110334125
2240478189240478190TC42GENIChomozygous110334129
2240478272240478273CG38GENIChomozygous110334131
2240478347240478348CT36GENIChomozygous110334132
2240478350240478351TC35GENIChomozygous110334134
2240478357240478358AG35GENIChomozygous110334136
2240468789240468789CC24GENIChomozygous127754135
2240472300240472301A24GENICpossibly homozygous127754136
2240472590240472590C44GENIChomozygous127754137
2240472807240472809TT55GENIChomozygous127754138
2240475523240475524G39GENIChomozygous127754139
2240477486240477488GT27GENICheterozygous127754140
2240478292240478314GCTTGCTTACCATGTGGGAAAG37GENIChomozygous127754141
2240468794240468795AC20GENIChomozygous120180116
2240470133240470134CT49GENIChomozygous111030853
2240470134240470135TG48GENIChomozygous110632299
2240479748240479749CT35GENIChomozygous110334138
2240479762240479762AA38GENIChomozygous127754142
2240479860240479861AG47GENICpossibly homozygous110334140
2240479895240479896CT61GENICpossibly homozygous110334142
2240480552240480553GC44GENIChomozygous120131634
2240480553240480554CA47GENICpossibly homozygous120131635