chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140542158140542159AG16GENIChomozygous69179231
7140543101140543102AG21GENIChomozygous69179234
7140543685140543686GA17GENICpossibly homozygous70407583
7140543695140543696CT20GENIChomozygous69179235
7140543889140543890AG26GENIChomozygous70407591
7140543909140543910TC22GENIChomozygous70407595
7140544212140544213AG35GENIChomozygous69179237
7140544334140544335CT20GENIChomozygous69179238
7140544417140544418GA28GENIChomozygous70407599
7140544697140544698TG8GENIChomozygous69179239
7140545330140545331TC18GENIChomozygous69179240
7140545331140545332GA18GENIChomozygous70407603
7140545641140545642GA22GENIChomozygous70407607
7140545980140545981CT8GENIChomozygous70407611