chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182749513027495131CT12GENIChomozygous110455437
182749683027496831CT15GENIChomozygous110455438
182749704427497045AC16GENIChomozygous110455439
182749708527497086GA18GENIChomozygous110455440
182749747127497472TC13GENIChomozygous110455441
182749780127497802AC10GENICpossibly homozygous110744810
182749786627497867CG11GENIChomozygous110455442
182750129327501294TC29GENIChomozygous110455443
182750137027501371AG25GENIChomozygous110455444
182750349127503492AG27GENIChomozygous110455445
182750453927504540CT36GENIChomozygous110455446
182750523527505236CT10GENIChomozygous110455447
182750552227505523TG22GENIChomozygous110455448
182751563527515636CT15GENIChomozygous110455449
182751594627515947AG9GENIChomozygous110455450
182751975727519758AG22GENIChomozygous110455451