chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3171013233171013234CA30GENIChomozygous112205368
3171013635171013635GCTG31GENIChomozygous131332724
3171014426171014427GT33GENIChomozygous112205370
3171014979171014980GA32GENIChomozygous112205372
3171014988171014989GA33GENIChomozygous112205374
3171015072171015073TA38GENIChomozygous112205376
3171017607171017608AT42GENIChomozygous112205378
3171017664171017665GA34GENIChomozygous112205380
3171017778171017779AG51GENIChomozygous112205382
3171021220171021221AG49GENIChomozygous112205384
3171022119171022120GA50GENIChomozygous112205386
3171022152171022153TG53GENICpossibly homozygous112205388
3171022817171022818GA46GENIChomozygous112205390
3171023037171023038AG48GENIChomozygous112205392
3171025463171025464GA46GENIChomozygous112205394
3171026720171026721GT44GENIChomozygous112205396
3171027491171027492GA52GENIChomozygous112205398
3171030259171030260GA48GENIChomozygous119686538
3171014816171014817TA34GENIChomozygous119653089
3171014816171014816AAAAC33GENIChomozygous127961064
3171021722171021722ATGTGAGCTCC48GENIChomozygous127961065
3171021603171021603T33GENICpossibly homozygous130915307
3171030256171030257G48GENIChomozygous130915308
3171026435171026436GA51GENIChomozygous112371401