chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56508314265083143GA22GENIChomozygous55432217
56508510665085107CT23GENICheterozygous55432233
56508587065085871TC1GENIChomozygous55432266
56508592165085922G-1GENIChomozygous55432278
56508592465085925AT2GENIChomozygous56217712
56508595165085952G-11GENIChomozygous55432280
56508756565087566GC16GENICpossibly homozygous55432290
56508862465088625AG20GENIChomozygous55432302
56508942665089427CT14GENIChomozygous56560708
56508992765089928AT9GENIChomozygous55432310
56509019065090191AT15GENICpossibly homozygous56560709
56509062865090629TC5GENIChomozygous55432316
56509160265091603TC16GENICpossibly homozygous55432324
56509268965092690TC20GENICpossibly homozygous55432328
56509328965093290TA12GENICheterozygous55432330
56509457865094579GA7GENIChomozygous56560710
56509472965094730CT15GENICpossibly homozygous55432334
56509490465094905AG21GENICpossibly homozygous55432336
56509535665095357GT18GENIChomozygous56560711
56509692765096928AG7GENICpossibly homozygous56560712
56509705465097055GA16GENICheterozygous55432350