chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2250711935250711936TA18GENIChomozygous110850746
2250713684250713685CG26GENIChomozygous110379613
2250714444250714445TG27GENICpossibly homozygous110850748
2250720073250720074GC31GENICheterozygous110915017
2250720077250720078GC32GENICheterozygous110915018
2250724143250724144TC13GENIChomozygous110379621
2250724390250724391CT19GENIChomozygous110379623
2250725150250725151CT7GENIChomozygous110850751
2250725211250725212AG11GENIChomozygous110379625
2250728211250728212AG19GENIChomozygous110379633
2250729247250729248TC16GENIChomozygous110850753
2250729654250729655GA17GENIChomozygous110379635
2250729893250729894GC31GENIChomozygous110379637
2250730274250730275GA30GENIChomozygous110379639
2250730508250730509TC25GENIChomozygous110379643
2250730986250730987CA15GENIChomozygous110379645
2250731668250731669TC17GENIChomozygous110379647
2250733489250733490CT12GENIChomozygous110379649
2250734415250734416TC18GENIChomozygous110850755
2250734722250734723AG12GENIChomozygous110379651
2250734870250734871AC13GENICpossibly homozygous110379653
2250735468250735469TC21GENIChomozygous110379655
2250736582250736583TC25GENIChomozygous110850757
2250737293250737294GA10GENIChomozygous110379657
2250737658250737659CT19GENIChomozygous110379659
2250737991250737992AC10GENIChomozygous110379661
2250738043250738044GT11GENIChomozygous110379663
2250742339250742340TA18GENIChomozygous110850759
2250742657250742658CG18GENIChomozygous110850761
2250743253250743254CA38GENIChomozygous110850763
2250743360250743361TG30GENIChomozygous110850765
2250744151250744152CT24GENIChomozygous110915020
2250732254250732255GC19GENIChomozygous110635630