chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3132823474132823475CG35GENIChomozygous609670550
3132824297132824298TTA14GENIChomozygous735117221
3132824969132824970CT16GENIChomozygous609670551
3132825168132825169A-11GENIChomozygous735117222
3132825181132825182CT11GENIChomozygous611612467
3132825538132825539TC23GENIChomozygous609670552
3132826314132826315TC32GENIChomozygous609670553
3132826526132826527GGA29GENIChomozygous735117223
3132826563132826564TC34GENIChomozygous609670554
3132827011132827012CG35GENIChomozygous609670555
3132827016132827017CG31GENIChomozygous611612468
3132827067132827068CCCT25GENIChomozygous735117224
3132827072132827073TC24GENIChomozygous611612469
3132827970132827971CG22GENIChomozygous609670556
3132828273132828274AG23GENIChomozygous609670557
3132828618132828619CCT13GENIChomozygous735117225
3132829043132829044TC21GENIChomozygous609670558
3132829648132829649T-16GENICpossibly homozygous735117226
3132830845132830846GGA7GENIChomozygous735117228
3132832452132832453CT29GENIChomozygous611612470
3132832616132832617GT19GENIChomozygous611612471