chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266257617266257618GA23GENIChomozygous108637750
1266259480266259481TG35GENIChomozygous108637751
1266259955266259956TC24GENIChomozygous108637752
1266260071266260072AC30GENIChomozygous108637753
1266260704266260705GA36GENIChomozygous108637754
1266260846266260847TA21GENIChomozygous108637755
1266261396266261397GC25GENIChomozygous108637756
1266262051266262052TC19GENIChomozygous108637757
1266262303266262304AG38GENIChomozygous108637758
1266262580266262581CT24GENIChomozygous108637759
1266263068266263069CA38GENIChomozygous108637760
1266264337266264338TA28GENIChomozygous108637761
1266264589266264590AG32GENIChomozygous108637762
1266265228266265229AG22GENIChomozygous108637763
1266266414266266415GT14GENIChomozygous108637764
1266266712266266713CT25GENIChomozygous108637765
1266267954266267955TC22GENIChomozygous108637766
1266268309266268310GA42GENIChomozygous108637767
1266270325266270326AG15GENIChomozygous108637768