chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103164798931647990TC54GENIChomozygous116547180
103165045131650452GT31GENIChomozygous116547182
103165168431651685TG41GENIChomozygous116547184
103165199731651998TG30GENIChomozygous116547188
103165253831652539TG11GENIChomozygous116547190
103165350931653510TC64GENIChomozygous116547192
103165478831654789TA67GENIChomozygous116547194
103165622331656224A59GENIChomozygous128803703
103165623731656238T55GENIChomozygous128803704
103165647531656475CCC53GENIChomozygous128803705
103165715331657154TA52GENIChomozygous116547196
103165826331658264CG41GENIChomozygous117002194
103165833131658331A34GENIChomozygous128803706
103165840731658409AT18GENIChomozygous128803707
103165841331658414TA18GENIChomozygous123436103
103165842231658422C20GENIChomozygous128803708
103165843531658435A24GENIChomozygous128803709
103165844531658445T24GENIChomozygous128803710
103165877431658775AG51GENIChomozygous116547198
103165877631658777GA51GENIChomozygous116547200
103165883131658832G46GENIChomozygous128803711
103165890531658906TC51GENIChomozygous116547202
103165903831659039TA40GENIChomozygous116547204
103165938931659390CT63GENIChomozygous116547206
103165943331659434TG60GENIChomozygous116547208
103165979331659794A53GENIChomozygous128803712
103165800331658004TC32GENIChomozygous117409178