chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5145194553145194554GA10GENIChomozygous56068634
5145196212145196213GC32GENIChomozygous55766652
5145196681145196682GA17GENICpossibly homozygous55766654
5145197357145197360AAG---11GENICheterozygous55766657
5145197359145197360G-18GENIChomozygous55766660
5145197372145197373CA19GENICpossibly homozygous55766663
5145201531145201532TTAA24GENIChomozygous55766669
5145201902145201903TC20GENIChomozygous55766672
5145202306145202307T-2GENIChomozygous55766677
5145202612145202613A-11GENIChomozygous56068635
5145203367145203368CCT23GENIChomozygous55766682
5145203482145203483AG23GENIChomozygous55766685
5145206857145206858CCAA17GENIChomozygous55766688
5145207717145207718AC19GENIChomozygous55766690
5145207821145207822T-7GENICheterozygous55766693
5145209812145209813GT15GENIChomozygous56125977
5145211568145211569GGT11GENIChomozygous55766696
5145211576145211577A-13GENIChomozygous55766699
5145211644145211645TA18GENIChomozygous55766702
5145211652145211653CA14GENIChomozygous55766707
5145211660145211661GA13GENIChomozygous55766710
5145211668145211669GA15GENIChomozygous55766713
5145212829145212830TA28GENIChomozygous55766719
5145212893145212894TC36GENIChomozygous55766721
5145213434145213435A-7GENIChomozygous55766729
5145215861145215862GGAAC10GENIChomozygous55766731
5145217673145217674CT14GENIChomozygous55766733
5145219076145219077T-8GENIChomozygous55766736