chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4156271325156271326GA48GENIChomozygous112902463
4156271347156271348CG42GENIChomozygous112902465
4156271635156271636GA33GENIChomozygous112902467
4156271904156271905TC20GENIChomozygous112902469
4156271909156271910CA24GENIChomozygous112902470
4156271915156271916CT22GENIChomozygous112902472
4156272501156272502TA30GENIChomozygous112902474
4156272889156272890AC61GENIChomozygous112902476
4156272902156272903GA63GENIChomozygous112902478
4156272909156272910TA59GENIChomozygous112902480
4156272943156272944TC63GENIChomozygous112902482
4156273464156273465CT31GENIChomozygous112902484
4156273800156273801CA38GENIChomozygous112902486
4156273880156273881CT39GENIChomozygous112902488
4156273929156273930AG40GENIChomozygous112902490
4156273975156273976AC49GENIChomozygous112902492
4156274049156274050AG68GENIChomozygous112902494
4156274206156274207TC48GENIChomozygous112902496
4156274709156274710AT48GENIChomozygous112902498
4156274885156274886TC43GENIChomozygous112902500
4156274928156274929TC40GENIChomozygous112902502
4156275273156275274TA19GENIChomozygous112902504
4156275340156275341CT21GENIChomozygous112902506
4156275372156275373CA27GENIChomozygous112902508
4156275533156275534CT42GENIChomozygous112902510
4156275668156275669TC52GENIChomozygous112902512
4156275689156275690CA53GENIChomozygous112902514
4156275780156275781CT38GENIChomozygous112902516