chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7119701430119701431AG54GENIChomozygous54082051
7119701440119701441GA59GENIChomozygous54082052
7119701543119701544CT59GENIChomozygous54082053
7119701611119701612AG30GENIChomozygous54082054
7119701995119701996CT50GENIChomozygous54082055
7119702044119702045C-32GENIChomozygous54082056
7119702046119702047CT35GENIChomozygous54920984
7119702090119702091CG38GENIChomozygous54082057
7119702157119702158CT26GENIChomozygous54082058
7119702344119702345TC40GENIChomozygous54082059
7119702691119702692GGGAGCCCGGAAGGCAACT51GENIChomozygous54082060
7119702748119702749TC51GENIChomozygous54082062
7119703416119703417AG42GENIChomozygous54082063
7119704199119704209ACACACACAC----------9GENICheterozygous55095773
7119704201119704209ACACACAC--------9GENICheterozygous55095775
7119705272119705273TC41GENIChomozygous54082064
7119706360119706361AG37INTERGENIChomozygous54082065
7119706498119706499GGACACACAC16INTERGENICpossibly homozygous54920986
7119706543119706544AC19INTERGENIChomozygous54082067
7119707003119707004TC33INTERGENIChomozygous54082068
7119708264119708268TCTG----7INTERGENICheterozygous55095779
7119708675119708676GA40INTERGENIChomozygous54082071
7119709472119709473A-21INTERGENIChomozygous54586999
7119710516119710517CCT11INTERGENIChomozygous54082073
7119713692119713693CT47INTERGENIChomozygous54082074
7119714298119714299AG38INTERGENIChomozygous54082075
7119715751119715752CT57INTERGENIChomozygous54082077
7119716047119716048AG29INTERGENIChomozygous54082078
7119708260119708268TCTGTCTG--------7INTERGENICheterozygous55361723