chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124347380443473805CT25GENICpossibly homozygous50211911
124347462043474621CCCA7GENIChomozygous50211912
124347466843474669CA26GENIChomozygous50211913
124347642643476427TC8GENICpossibly homozygous50211916
124348008943480090AG26GENIChomozygous50211924