chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3171013233171013234CA37GENICpossibly homozygous112205368
3171013635171013635GCTG20GENIChomozygous131332724
3171014426171014427GT24GENIChomozygous112205370
3171014979171014980GA10GENIChomozygous112205372
3171014988171014989GA8GENIChomozygous112205374
3171015072171015073TA14GENIChomozygous112205376
3171017607171017608AT31GENIChomozygous112205378
3171017664171017665GA28GENIChomozygous112205380
3171017778171017779AG30GENIChomozygous112205382
3171021220171021221AG25GENIChomozygous112205384
3171022119171022120GA37GENIChomozygous112205386
3171022152171022153TG37GENIChomozygous112205388
3171022817171022818GA26GENIChomozygous112205390
3171023037171023038AG31GENIChomozygous112205392
3171025463171025464GA25GENIChomozygous112205394
3171026720171026721GT33GENIChomozygous112205396
3171027491171027492GA42GENIChomozygous112205398
3171030259171030260GA28GENIChomozygous119686538
3171014816171014817TA37GENIChomozygous119653089
3171014816171014816AAAAC35GENIChomozygous127961064
3171021722171021722ATGTGAGCTCC32GENIChomozygous127961065
3171021603171021603T35GENIChomozygous130915307
3171030256171030257G27GENIChomozygous130915308
3171026435171026436GA30GENIChomozygous112371401