chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17759135877591359CT38GENIChomozygous142830607
17759229577592296AG47GENIChomozygous142830608
17759232277592323AG43GENIChomozygous142830609
17759325277593253TC14GENIChomozygous142830610
17759465577594656C37GENIChomozygous142787831
17759719777597198C7GENIChomozygous142787832
17759769177597692AG38GENIChomozygous142830611
17759772977597730CG43GENICpossibly homozygous142830612