chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108415849108415872GAGCAGAGCGGCCTCTGCAGTGT30GENIChomozygous128859576
10108416220108416221TC51GENIChomozygous116715850
10108417681108417682TA55GENIChomozygous116715852
10108418482108418483CT39GENICpossibly homozygous116715854
10108418484108418485GC39GENICpossibly homozygous116715856
10108418486108418488TC40GENICpossibly homozygous128859577
10108418849108418850AG48GENIChomozygous116715858
10108418900108418901TC50GENIChomozygous116715861
10108420294108420295GC56GENIChomozygous116715863
10108421473108421474CT31GENIChomozygous116715865
10108422041108422042AG38GENIChomozygous116715867
10108423745108423746AC48GENIChomozygous116715869