chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228405489228405490AG26GENIChomozygous61603711
1228405720228405721CT17GENIChomozygous61603712
1228406740228406742CT--15GENIChomozygous61603713
1228407166228407167TTGTTTATTTATTC11GENIChomozygous62250512
1228407174228407175TTATTC10GENIChomozygous62250513
1228407361228407362CT13GENIChomozygous61603721
1228407391228407392TA16GENIChomozygous61603722
1228407589228407590CT12GENIChomozygous61603723
1228408093228408094GGTATGA9GENIChomozygous61603726
1228408252228408253GA16GENIChomozygous61603727
1228408708228408709AAGACT11GENIChomozygous61603736
1228408958228408959TC34GENIChomozygous61603737
1228409188228409189TC12GENIChomozygous61603738
1228409250228409251T-18GENIChomozygous61603739
1228409252228409253GC18GENIChomozygous62250514
1228409351228409352G-16GENIChomozygous61603741
1228409780228409781AG16GENIChomozygous61603742
1228409798228409799TG20GENIChomozygous61603743
1228409822228409823CCT21GENIChomozygous61603744
1228410725228410726CCTT3GENIChomozygous62276013
1228411186228411187CT25GENIChomozygous61603745
1228411674228411675TC27GENIChomozygous61603746
1228411781228411783CA--26GENIChomozygous61603747
1228411941228411942AG23GENIChomozygous61603748
1228413481228413482GA24GENIChomozygous61603749
1228413849228413850AAGAGCTGAGGCTGAGGGAGCACGAAGCTGAGGGAGCACG30GENIChomozygous62485961
1228414795228414796AG25GENIChomozygous61603753
1228414863228414864AG19GENIChomozygous61603754
1228414932228414933CT13GENIChomozygous61603755
1228416532228416533AG20GENIChomozygous61603756
1228417186228417187TC22GENIChomozygous61603757
1228418063228418064CT19GENIChomozygous61603758