chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5140522736140522737TC31GENIChomozygous55752321
5140523268140523269TC39GENIChomozygous55752322
5140523895140523896GA27GENICpossibly homozygous55752323
5140524357140524358CA29GENIChomozygous55752324
5140524484140524485GA28GENICpossibly homozygous55752325
5140526791140526792GA28GENIChomozygous56235069
5140527096140527097AG35GENIChomozygous55752327
5140528279140528280AC43GENIChomozygous55752328
5140528460140528461CT38GENIChomozygous55752329
5140529390140529391TC36GENIChomozygous55752330
5140529621140529622AG34GENIChomozygous55752331
5140529859140529860CT40GENIChomozygous55752332
5140529961140529962GA20GENIChomozygous55752333
5140531305140531306CCA10GENIChomozygous56493876
5140531308140531309CCAAACAAA10GENIChomozygous56493877
5140533067140533068AG27GENIChomozygous56235071
5140533495140533496AAG21GENICpossibly homozygous56235072
5140534008140534009GA34GENICpossibly homozygous55752340
5140534346140534347GA34GENIChomozygous56235073
5140535945140535946GA31GENIChomozygous55752341
5140536816140536817AG31GENIChomozygous55752343
5140537546140537547CA26GENIChomozygous55752344