chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4159430970159430971CT53GENIChomozygous132467785
4159434863159434863ATATACATACATATGTACATATACATACATATATACATATACATACATATACATACATATGTACATATACATACATATAC25GENIChomozygous128097591
4159437517159437518T44GENIChomozygous128097592
4159447514159447518ACCA11GENICheterozygous132296240
4159447525159447526CT10GENICheterozygous132467786
4159447914159447914T7GENIChomozygous128097595
4159447932159447932C10GENIChomozygous128097596
4159447946159447947T10GENIChomozygous128097597
4159447960159447960G10GENIChomozygous128097598
4159447969159447970G14GENIChomozygous128097599
4159447991159447991G17GENIChomozygous128097600
4159455666159455667TG42GENIChomozygous112912828