chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403357914033583TTTT----20GENICpossibly homozygous769335772
101403406114034062TC18GENIChomozygous672006029
101403420714034208AAAT1GENIChomozygous769335774
101403433814034339A-8GENIChomozygous769335775
101403462714034628GA21GENIChomozygous672006030
101403486914034870CA33GENIChomozygous672006031
101403531614035319AAA---7GENICheterozygous769335776
101403531714035319AA--7GENICheterozygous769335777
101403675914036760A-21GENICpossibly homozygous769335779
101403733314037334GC27GENIChomozygous672006032
101403920514039206TC28GENIChomozygous672006033
101404104614041054GTGTGTGT--------19GENICheterozygous769335780
101404104814041054GTGTGT------19GENICheterozygous769335781
101404111414041115AATGTGTGTGTAGTATGTGG20GENIChomozygous769335784
101404375314043754AG24GENIChomozygous672006034
101404423614044237TC28GENIChomozygous672006035
101404493714044941TTTG----19GENIChomozygous769335785
101404532914045330GA20GENIChomozygous672006036
101404540014045401TTTCCTGGGAGC23GENIChomozygous769335787