chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1169903053169903054CA69GENIChomozygous108371219
1169903270169903271GA41GENIChomozygous108371221
1169903472169903473AC67GENICpossibly homozygous108371223
1169903660169903661CT38GENIChomozygous108371225
1169903780169903781TG52GENIChomozygous108371227
1169903824169903825CT42GENIChomozygous108371229
1169903904169903905CT42GENIChomozygous108371231