chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108697497986974980TA12GENICpossibly homozygous82720887
108697498086974981CA9GENIChomozygous82720888
108697499186974992AT7GENIChomozygous68143767
108698977086989771TA19GENIChomozygous68143815
108699144986991450GT20GENIChomozygous68928232
108699254786992548GT24GENIChomozygous68928234
108699389986993900TC28GENIChomozygous68143836
108699607886996079AG16GENIChomozygous82720889
108699608386996084GA13GENIChomozygous68928236
108699617186996172AT19GENICpossibly homozygous68928238
108699618186996182TC20GENIChomozygous68143856
108699624686996247CG22GENIChomozygous68928240
108699658386996584AG23GENIChomozygous68928242
108699830986998310AT31GENIChomozygous69145171
108700088987000890AG18GENIChomozygous68143865
108700609187006092AG23GENIChomozygous68143871
108700762787007628CA22GENICheterozygous82704446
108700946587009466CT21GENICheterozygous82704447
108701940987019410AG21GENICheterozygous82704453
108702468887024689GA38GENIChomozygous68143901
108702482587024826TC27GENICheterozygous82704454
108700602287006023GA17GENIChomozygous68444963