chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242322324232233TC27GENICpossibly homozygous545991679
1242327264232727AG6GENIChomozygous545991680
1242338354233836GC11GENICpossibly homozygous545991681
1242338884233889GA10GENIChomozygous545991682
1242340884234089TC12GENIChomozygous545991683
1242343054234306TC20GENICpossibly homozygous545991684
1242344524234453TC4GENIChomozygous545991685
1242350874235088TG18GENIChomozygous545991686
1242355454235546GC13GENIChomozygous545991687
1242358524235853CA16GENIChomozygous545991688
1242359274235928TC17GENIChomozygous545991689
1242359854235986TC11GENIChomozygous545991690
1242373164237317GT23GENICheterozygous545991691
1242374124237413TTGGTTATTCAACTCGACCTTTGAA2GENICheterozygous698437645
1242374454237446AAT6GENIChomozygous698437646
1242374524237453GA8GENIChomozygous545991692
1242396454239646TA17GENIChomozygous545991693
1242401504240151CCT3GENIChomozygous698437647
1242420704242071T-16GENICpossibly homozygous698437648
1242454294245430GGAC10GENICheterozygous698437649
1242455704245571TTAC5GENICheterozygous698437650
1242519794251980AG15GENIChomozygous545991694
1242555614255562CT15GENIChomozygous545991695
1242570074257008GA2GENIChomozygous545991696
1242590844259085GA12GENICpossibly homozygous545991697