chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266257617266257618GA23GENIChomozygous963027577
1266259480266259481TG35GENIChomozygous963027578
1266259955266259956TC24GENIChomozygous963027579
1266260071266260072AC30GENIChomozygous963027580
1266260704266260705GA36GENIChomozygous963027581
1266260846266260847TA21GENIChomozygous963027582
1266261396266261397GC25GENIChomozygous963027583
1266262051266262052TC19GENIChomozygous963027584
1266262303266262304AG38GENIChomozygous963027585
1266262580266262581CT24GENIChomozygous963027586
1266263068266263069CA38GENIChomozygous963027587
1266264337266264338TA28GENIChomozygous963027588
1266264589266264590AG32GENIChomozygous963027589
1266265228266265229AG22GENIChomozygous963027590
1266266414266266415GT14GENIChomozygous963027591
1266266712266266713CT25GENIChomozygous963027592
1266267954266267955TC22GENIChomozygous963027593
1266268309266268310GA42GENIChomozygous963027594
1266270325266270326AG15GENIChomozygous963027595