chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108264969182649692CT25GENIChomozygous51518112
108264970782649708CA26GENICpossibly homozygous51518113
108264990782649908AT35GENIChomozygous51518114
108265071182650712TC26GENIChomozygous51518115
108265158282651583A-23GENIChomozygous51518116
108265246682652478ACACACACACAC------------23GENIChomozygous51518119
108265311082653122GTGTGTGTGTGT------------5GENIChomozygous52603151
108265346082653461AATG24GENIChomozygous51518122
108265370382653704TC28GENIChomozygous51518123
108265519482655195TC38GENIChomozygous51518124
108265534582655346AT16GENIChomozygous51518125
108265582982655830CT28GENIChomozygous51518126
108265665182656652GT33GENIChomozygous51518127
108265675982656760TA30GENIChomozygous51518128
108265787682657877GA20GENIChomozygous51518129
108265799082657991TTACAC17GENICheterozygous51518130
108265799082657991TTACACACACACAC17GENICpossibly homozygous52506324
108265930382659304CT30GENIChomozygous51518131
108265977482659775TC28GENIChomozygous51518132
108266034382660344TC20GENIChomozygous51518133
108266038182660382AG20GENIChomozygous51518134
108266060782660608A-34GENIChomozygous51518135
108266241882662419GA19GENIChomozygous51518136