chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3171013233171013234CA22GENIChomozygous112205368
3171013635171013635GCTG15GENIChomozygous131332724
3171014426171014427GT14GENIChomozygous112205370
3171014816171014817TA17GENIChomozygous119653089
3171014816171014816AAAAC16GENIChomozygous127961064
3171014979171014980GA13GENIChomozygous112205372
3171014988171014989GA14GENIChomozygous112205374
3171015072171015073TA18GENIChomozygous112205376
3171017607171017608AT11GENIChomozygous112205378
3171017664171017665GA19GENIChomozygous112205380
3171017778171017779AG18GENIChomozygous112205382
3171021220171021221AG12GENIChomozygous112205384
3171021722171021722ATGTGAGCTCC16GENIChomozygous127961065
3171022119171022120GA15GENIChomozygous112205386
3171022152171022153TG16GENIChomozygous112205388
3171022817171022818GA18GENIChomozygous112205390
3171023037171023038AG15GENIChomozygous112205392
3171025463171025464GA14GENIChomozygous112205394
3171026435171026436GA21GENIChomozygous112371401
3171026720171026721GT27GENIChomozygous112205396
3171027491171027492GA21GENIChomozygous112205398
3171030259171030260GA22GENIChomozygous119686538
3171030256171030257G21GENIChomozygous130915308
3171021603171021603T8GENIChomozygous130915307