chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2240467983240467984CT19GENIChomozygous110334098
2240468789240468789CC22GENIChomozygous127754135
2240468794240468795AC24GENIChomozygous120180116
2240470124240470125CT9GENIChomozygous110334099
2240470450240470451AG21GENIChomozygous110334102
2240471400240471401CA24GENIChomozygous110334104
2240471579240471580TC20GENIChomozygous110334106
2240471735240471736CA12GENIChomozygous110334108
2240472260240472261TC16GENIChomozygous110334110
2240472300240472301A14GENICpossibly homozygous127754136
2240472376240472377AC18GENIChomozygous110334111
2240472590240472590C16GENIChomozygous127754137
2240472807240472809TT8GENIChomozygous127754138
2240472811240472812GC9GENIChomozygous110334113
2240473575240473576GA24GENIChomozygous110334115
2240473628240473629GA30GENIChomozygous110334117
2240473762240473763AG23GENIChomozygous110334119
2240473903240473904AG17GENIChomozygous110334121
2240475341240475342GA21GENIChomozygous110334123
2240475523240475524G15GENIChomozygous127754139
2240475780240475781AG20GENIChomozygous110334125
2240478189240478190TC13GENIChomozygous110334129
2240478272240478273CG15GENIChomozygous110334131
2240478292240478314GCTTGCTTACCATGTGGGAAAG17GENIChomozygous127754141
2240478347240478348CT17GENIChomozygous110334132
2240478350240478351TC16GENIChomozygous110334134
2240478357240478358AG15GENIChomozygous110334136
2240479748240479749CT20GENIChomozygous110334138
2240479762240479762AA16GENIChomozygous127754142
2240479860240479861AG16GENIChomozygous110334140
2240479895240479896CT10GENIChomozygous110334142
2240480553240480554CA18GENIChomozygous120131635
2240470133240470134CT9GENIChomozygous111030853
2240470134240470135TG9GENIChomozygous110632299
2240480552240480553GC19GENIChomozygous120131634