chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181903614519036146TA36GENIChomozygous110811718
181903627019036271GA35GENICpossibly homozygous110811720
181903674619036747CA38GENIChomozygous110811722
181903857919038580GC47GENIChomozygous110530066
181903996819039969TC42GENIChomozygous110530068
181904031719040318CT64GENIChomozygous110811724
181904073919040740GA24GENIChomozygous110811726
181904100619041007CG40GENIChomozygous110811728
181904161419041615TA43GENIChomozygous110811730
181904148919041490CA64GENIChomozygous110293508
181903897219038973CT37GENIChomozygous110293506
181904331319043314GA34GENIChomozygous110578421