chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5140522736140522737TC21GENIChomozygous55752321
5140523268140523269TC32GENIChomozygous55752322
5140523895140523896GA7GENIChomozygous55752323
5140524357140524358CA15GENIChomozygous55752324
5140524484140524485GA14GENIChomozygous55752325
5140526791140526792GA22GENIChomozygous56235069
5140527096140527097AG17GENIChomozygous55752327
5140528279140528280AC5GENIChomozygous55752328
5140528460140528461CT13GENIChomozygous55752329
5140529390140529391TC28GENIChomozygous55752330
5140529621140529622AG22GENIChomozygous55752331
5140529859140529860CT13GENIChomozygous55752332
5140529961140529962GA12GENIChomozygous55752333
5140533067140533068AG21GENIChomozygous56235071
5140533495140533496AAG5GENIChomozygous56235072
5140534008140534009GA24GENIChomozygous55752340
5140534346140534347GA26GENIChomozygous56235073
5140535945140535946GA16GENICpossibly homozygous55752341
5140536816140536817AG14GENIChomozygous55752343
5140537546140537547CA6GENIChomozygous55752344
5140531308140531309CCAAACAAA9GENIChomozygous56493877
5140531305140531306CCA9GENIChomozygous56493876