chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403357914033583TTTT----17GENICheterozygous51622641
101403406114034062TC14GENICpossibly homozygous51622644
101403420714034208AAAT3GENIChomozygous51622645
101403433814034339A-10GENICpossibly homozygous51622646
101403462714034628GA20GENIChomozygous51622647
101403486914034870CA26GENIChomozygous51622648
101403531614035319AAA---5GENICheterozygous52431569
101403531714035319AA--5GENICheterozygous52431571
101403675914036760A-29GENICpossibly homozygous51622650
101403733314037334GC30GENIChomozygous51622651
101403920514039206TC13GENIChomozygous51622652
101404104614041054GTGTGTGT--------11GENICheterozygous52481274
101404104814041054GTGTGT------11GENICheterozygous52481276
101404111414041115AATGTGTGTGTAGTATGTGG9GENIChomozygous52313039
101404375314043754AG22GENIChomozygous51622655
101404423614044237TC35GENIChomozygous51622656
101404493714044941TTTG----17GENIChomozygous51622657
101404532914045330GA26GENIChomozygous51622658
101404540014045401TTTCCTGGGAGC16GENIChomozygous51622659