chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167424029774240298CA15GENIChomozygous814107056
167424121074241211TC53GENICheterozygous814107057
167424123874241239TC48GENICpossibly homozygous814107058
167424173074241731CA31GENIChomozygous814107059
167424255674242557CT58GENIChomozygous814107060
167424265074242651AG47GENIChomozygous814107061
167424438274244383AG34GENICpossibly homozygous814107062
167424514274245143CT21GENIChomozygous814107063
167424645274246453TA20GENIChomozygous814107064
167424807374248074CT25GENIChomozygous814107065
167425066974250670AG21GENIChomozygous814107066
167425249174252492GA32GENIChomozygous814107067
167425312574253126AG40GENIChomozygous814107068
167425342874253429AT27GENIChomozygous814107069
167425454574254546GA26GENICpossibly homozygous814107070
167425493774254938GA35GENIChomozygous814107071
167425592574255926AG42GENIChomozygous814107072
167425594274255943TC42GENIChomozygous814107073
167425629174256292AG38GENIChomozygous814107074
167425644874256449CT42GENIChomozygous814107075
167425650374256504TC42GENIChomozygous814107076
167425665574256656GA33GENIChomozygous814107077
167425689774256898CT32GENIChomozygous814107078
167425851374258514AG33GENIChomozygous814107079
167425921274259213AG36GENIChomozygous814107080
167425995974259960AT27GENIChomozygous814107081