chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1654889216548908TCTATCTATCTATCTA----------------8GENIChomozygous726268553
X1655217016552171T-9GENIChomozygous726268557
X1655531916555320CT24GENIChomozygous591908724
X1655826716558271ACAC----1GENIChomozygous726268561
X1655897316558974AG13GENIChomozygous591908725
X1655942116559422TC8GENIChomozygous591908726
X1656013816560139AAT7GENIChomozygous726268562
X1656087516560876CT20GENIChomozygous591908727
X1656114416561145CT14GENIChomozygous591908728
X1656133916561342AAT---15GENIChomozygous726268563
X1656182516561826GC11GENIChomozygous591908729
X1656212016562121AC9GENICpossibly homozygous591908730
X1656212216562123AC9GENIChomozygous594612929
X1656307416563075AG12GENIChomozygous591908731
X1656421116564212AAGG9GENIChomozygous726268564
X1656421616564217AG13GENIChomozygous594612930