chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1655217016552171T-37GENICpossibly homozygous45330970
X1655531916555320CT48GENIChomozygous45274444
X1655703316557034CCAT49GENICpossibly homozygous45274446
X1655897316558974AG34GENIChomozygous45330971
X1655942116559422TC47GENIChomozygous45274449
X1656013816560139AAT32GENIChomozygous45274450
X1656087516560876CT27GENIChomozygous45330972
X1656114416561145CT42GENIChomozygous45330973
X1656133916561342AAT---46GENIChomozygous45330974
X1656182516561826GC37GENICpossibly homozygous45330975
X1656211416562115TTC14GENICheterozygous45274452
X1656212016562121AC20GENIChomozygous45330976
X1656212216562123AC19GENIChomozygous45330977
X1656307416563075AG40GENIChomozygous45330978
X1656421116564212AAGG21GENIChomozygous45330979