chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4156271325156271326GA10GENIChomozygous112902463
4156271347156271348CG9GENIChomozygous112902465
4156271426156271427CT11GENIChomozygous113399709
4156271635156271636GA12GENIChomozygous112902467
4156271904156271905TC6GENIChomozygous112902469
4156272501156272502TA8GENIChomozygous112902474
4156272889156272890AC10GENIChomozygous112902476
4156272902156272903GA9GENIChomozygous112902478
4156272909156272910TA10GENIChomozygous112902480
4156272943156272944TC14GENIChomozygous112902482
4156273464156273465CT9GENIChomozygous112902484
4156273880156273881CT11GENIChomozygous112902488
4156273929156273930AG10GENIChomozygous112902490
4156273975156273976AC19GENIChomozygous112902492
4156274049156274050AG6GENIChomozygous112902494
4156274206156274207TC19GENIChomozygous112902496
4156274709156274710AT16GENIChomozygous112902498
4156274885156274886TC10GENIChomozygous112902500
4156274898156274899CG12GENIChomozygous113399711
4156275273156275274TA9GENIChomozygous112902504
4156275340156275341CT9GENIChomozygous112902506
4156275454156275455AG10GENIChomozygous113399714
4156275561156275562AT18GENIChomozygous113399716
4156275736156275737TC13GENIChomozygous113399718
4156275969156275970AG18GENIChomozygous113399720
4156276052156276053TC15GENIChomozygous113399722