chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101381609713816098CCACTCCGAAGAGGCAGCTCCCCT29GENIChomozygous703661555
101381615313816154AG30GENIChomozygous556964523
101381689013816891GGGTGTGT5GENICheterozygous703661556
101381689013816891GGGTGTGTGT5GENICheterozygous703661557
101381704213817043AG19GENIChomozygous556964524
101381816313818164GGC10GENICpossibly homozygous703661559
101381836213818363GA16GENIChomozygous556964525
101381886213818863CCA20GENIChomozygous703661560
101381920013819201A-24GENIChomozygous703661561