chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5140522736140522737TC25GENIChomozygous55752321
5140523268140523269TC30GENIChomozygous55752322
5140523895140523896GA19GENIChomozygous55752323
5140524357140524358CA29GENICpossibly homozygous55752324
5140524484140524485GA32GENICpossibly homozygous55752325
5140526791140526792GA29GENIChomozygous56235069
5140527096140527097AG32GENIChomozygous55752327
5140528279140528280AC35GENIChomozygous55752328
5140528460140528461CT34GENIChomozygous55752329
5140529390140529391TC33GENIChomozygous55752330
5140529621140529622AG33GENIChomozygous55752331
5140529859140529860CT25GENIChomozygous55752332
5140529961140529962GA22GENIChomozygous55752333
5140533067140533068AG20GENIChomozygous56235071
5140533495140533496AAG4GENIChomozygous56235072
5140534008140534009GA34GENIChomozygous55752340
5140534346140534347GA35GENIChomozygous56235073
5140535945140535946GA29GENIChomozygous55752341
5140536816140536817AG21GENIChomozygous55752343
5140537546140537547CA20GENIChomozygous55752344
5140531308140531309CCAAACAAA21GENICpossibly homozygous56493877
5140531305140531306CCA21GENICpossibly homozygous56493876