chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265506921265506922CT38GENICpossibly homozygous108637134
1265507196265507197CT41GENIChomozygous109377912
1265507749265507750TG63GENIChomozygous108637135
1265510911265510912AG56GENIChomozygous108637137
1265510999265511000TC57GENIChomozygous108637138
1265512257265512258TA63GENIChomozygous109377914
1265515622265515622A49GENIChomozygous134390968
1265520609265520609C25GENICpossibly homozygous134390969
1265523242265523243AG41GENIChomozygous109377916