chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1243354543243354544CA17GENICpossibly homozygous135852702
1243354766243354767GA20GENIChomozygous135852703
1243354777243354778CT20GENIChomozygous135852704
1243355087243355088AC18GENIChomozygous141305557
1243357035243357036GC14GENIChomozygous141305558
1243358061243358062TC17GENIChomozygous135852706
1243358286243358286CCT7GENICpossibly homozygous135469783
1243358364243358365TC9GENIChomozygous135852707
1243358904243358905GA20GENIChomozygous141305559
1243358971243358972AC15GENIChomozygous141305560
1243359350243359351AG14GENIChomozygous135852708
1243359797243359798GA17GENIChomozygous141305561
1243358340243358346CTCCTC9GENIChomozygous141181114
1243360762243360763TC13GENIChomozygous135852710
1243361243243361244GA24GENIChomozygous135852711
1243362637243362638AG18GENIChomozygous135852712
1243365432243365433AT13GENIChomozygous144574298
1243365433243365434TC13GENIChomozygous144574299
1243368341243368353TGTGTGTGTGTT10GENIChomozygous144530219