chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5140522736140522737TC21GENIChomozygous55752321
5140523268140523269TC9GENIChomozygous55752322
5140523895140523896GA24GENICpossibly homozygous55752323
5140524357140524358CA21GENICpossibly homozygous55752324
5140524484140524485GA22GENICpossibly homozygous55752325
5140525288140525289GA14GENICpossibly homozygous55752326
5140527096140527097AG20GENICpossibly homozygous55752327
5140528279140528280AC10GENIChomozygous55752328
5140528460140528461CT22GENIChomozygous55752329
5140529390140529391TC19GENIChomozygous55752330
5140529621140529622AG19GENIChomozygous55752331
5140529859140529860CT19GENIChomozygous55752332
5140529961140529962GA7GENIChomozygous55752333
5140531312140531314CC--11GENIChomozygous55752335
5140531315140531321ACCAAC------15GENIChomozygous55752336
5140531332140531333AC11GENIChomozygous55752338
5140534008140534009GA16GENIChomozygous55752340
5140535945140535946GA22GENIChomozygous55752341
5140536615140536616GA16GENICpossibly homozygous55752342
5140536816140536817AG17GENIChomozygous55752343
5140537546140537547CA18GENICpossibly homozygous55752344