chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130007320130007321TG41GENIChomozygous54110045
7130007450130007451GA30GENICpossibly homozygous54110046
7130008122130008123CA20GENIChomozygous54110047
7130008199130008200CT30GENIChomozygous54110048
7130008272130008273CT13GENIChomozygous54110049
7130008467130008468AC37GENICpossibly homozygous54110050
7130009564130009565TC64GENIChomozygous54110053
7130008963130008964CT39GENIChomozygous54110051
7130009502130009503TG61GENICpossibly homozygous54110052
7130009628130009629TA65GENIChomozygous54110054
7130009970130009971GGC4GENIChomozygous54110055
7130009976130009977GC16GENIChomozygous54110056
7130009981130009982TC15GENIChomozygous54110057
7130010067130010068GA29GENIChomozygous54110058
7130010091130010092CT30GENIChomozygous54110059
7130010247130010248CT33GENICpossibly homozygous54110060
7130010305130010306CA28GENICpossibly homozygous54110061
7130010709130010710GA42GENICpossibly homozygous54110062
7130010727130010728TC44GENICpossibly homozygous54110063
7130011098130011099CT47GENIChomozygous54110064
7130011398130011399CT48GENICpossibly homozygous54110065
7130011637130011638CT25GENICpossibly homozygous54110066
7130011760130011761CT32GENIChomozygous54110067