chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2193436942193436943GT22GENIChomozygous110183075
2193437390193437391TA21GENIChomozygous110183076
2193437802193437803GC16GENIChomozygous110183077
2193438447193438448TC11GENIChomozygous110183078
2193438645193438646CT19GENIChomozygous110183079
2193438646193438647GA18GENIChomozygous110183080
2193439176193439177TG26GENIChomozygous110183081
2193439782193439783AG21GENIChomozygous110183082
2193440091193440092TC13GENIChomozygous110183083
2193440099193440100AC16GENIChomozygous110183084
2193440319193440320GA9GENIChomozygous110183085
2193440571193440572GA19GENIChomozygous110183086
2193440668193440669CA26GENIChomozygous110183087
2193441026193441027GA25GENIChomozygous110183088
2193444774193444775TC12GENIChomozygous110183092
2193445725193445726GT17GENIChomozygous110183093
2193445996193445997GA12GENIChomozygous110183094
2193446025193446026CA13GENIChomozygous110183095
2193455809193455810AG18GENIChomozygous110183102
2193456480193456481GA22GENIChomozygous110183103
2193457370193457371AT24GENIChomozygous110183104
2193457424193457425AC27GENIChomozygous110183105