chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142034399620343997GT28GENIChomozygous139470690
142034986620349867GC15GENIChomozygous139470691
142034995220349953GA11GENIChomozygous139470692
142035008020350081GA20GENIChomozygous139470693
142035331520353316GT21GENIChomozygous139470694
142035517420355175CT22GENIChomozygous139470695
142035541720355418AG17GENIChomozygous139470696
142035561320355617ATGT13GENIChomozygous139383469
142035146520351465A15GENICpossibly homozygous139383466
142035215120352152T15GENIChomozygous139383467
142035505820355059T20GENIChomozygous139383468
142035711220357114TA18GENICheterozygous139383470
142035711320357114AG18GENICheterozygous403354232
142035711620357117C18GENICheterozygous403354234
142035711620357117CT18GENICheterozygous403354233
142035711320357114A18GENICheterozygous403354231
142035712920357130AG24GENIChomozygous403354235
142035712920357130A24GENICheterozygous403354236