chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187217902972179030AC4GENIChomozygous46511693
187217950572179506GA13GENICpossibly homozygous46668062
187217973372179734AG10GENIChomozygous46668063
187218007572180076AG9GENIChomozygous46668064
187218008672180087AG4GENIChomozygous46668065
187218012572180126AG11GENIChomozygous46668066
187218061972180620GT19GENIChomozygous46668067
187218131372181314CT14GENICpossibly homozygous46668068
187218160672181607AT7GENIChomozygous46511696
187218174472181745TC15GENIChomozygous46668069
187218214872182149TG12GENICpossibly homozygous46511697
187218230272182303GA16GENIChomozygous46668071
187218317472183183TCCTTTCCC---------3GENICheterozygous46511700
187218388672183887AG9GENICpossibly homozygous46511703
187218487572184876CT19GENIChomozygous46668074
187218496472184965TC11GENICheterozygous46511704
187218543172185432TC21GENICpossibly homozygous46511705
187218588872185889GA22GENICpossibly homozygous46668075
187218610272186103TC12GENIChomozygous46668076
187218610972186110CT12GENIChomozygous46668077
187218701772187018TC11GENIChomozygous46511709
187218702472187025CT14GENICpossibly homozygous46668078
187218706872187069GA13GENIChomozygous46668079
187218726672187267TC14GENICpossibly homozygous46668080
187219069472190695AAT3GENICheterozygous46668081
187223585772235858GC4GENIChomozygous46511716