chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5140522736140522737TC11GENIChomozygous55752321
5140523268140523269TC13GENICpossibly homozygous55752322
5140523895140523896GA11GENICpossibly homozygous55752323
5140524357140524358CA14GENICpossibly homozygous55752324
5140524484140524485GA11GENICpossibly homozygous55752325
5140525288140525289GA11GENICheterozygous55752326
5140527096140527097AG11GENICpossibly homozygous55752327
5140528279140528280AC7GENIChomozygous55752328
5140528460140528461CT6GENIChomozygous55752329
5140529390140529391TC12GENICpossibly homozygous55752330
5140529621140529622AG14GENICpossibly homozygous55752331
5140529859140529860CT17GENICheterozygous55752332
5140529961140529962GA2GENICheterozygous55752333
5140531312140531314CC--10GENICheterozygous55752335
5140531315140531321ACCAAC------11GENICheterozygous55752336
5140531332140531333AC8GENICpossibly homozygous55752338
5140534008140534009GA12GENICpossibly homozygous55752340
5140535945140535946GA17GENICpossibly homozygous55752341
5140536615140536616GA7GENIChomozygous55752342
5140536816140536817AG8GENIChomozygous55752343
5140537546140537547CA1GENIChomozygous55752344