chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1099120129912013TC2GENIChomozygous51616110
1099120209912021TC2GENIChomozygous51616111
1099124599912460AG15GENIChomozygous52027443
1099131249913125TG20GENIChomozygous52027445
1099131659913166GA23GENIChomozygous52027447
1099132619913262AT24GENIChomozygous52027449
1099133449913345AG22GENIChomozygous51616114
1099136979913698GT31GENIChomozygous51616115
1099139609913961G-15GENIChomozygous52027453
1099141189914119CT24GENIChomozygous52027455
1099141409914141G-29GENIChomozygous52027457
1099141919914192AG26GENIChomozygous51616117
1099142209914221GT21GENIChomozygous52027459
1099144759914476AG32GENIChomozygous51616118
1099152549915255TTC23GENIChomozygous51616121
1099163029916303A-17GENIChomozygous52027461
1099164289916437AGAGCAGTC---------24GENIChomozygous52027463
1099164509916451TA25GENIChomozygous51616124
1099177599917760AG21GENIChomozygous51616126
1099188409918841CT25GENIChomozygous52027465
1099188499918850TC24GENIChomozygous52027467
1099189969918997TC10GENIChomozygous52027469
1099191649919165TC25GENIChomozygous52027471
1099136679913668CA30GENIChomozygous51323666
1099165929916593TTC15GENIChomozygous51323667
1099183239918324AG28GENIChomozygous51323669
1099142579914258AG26GENIChomozygous52239032
1099168009916801GA19GENIChomozygous52239034
1099181059918106GA38GENIChomozygous52239036