chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403357914033583TTTT----12GENICpossibly homozygous51622641
101403406114034062TC13GENIChomozygous51622644
101403420714034208AAAT1GENIChomozygous51622645
101403433814034339A-9GENIChomozygous51622646
101403462714034628GA10GENIChomozygous51622647
101403486914034870CA15GENIChomozygous51622648
101403531614035319AAA---4GENICheterozygous52431569
101403531714035319AA--4GENICheterozygous52431571
101403675914036760A-22GENICpossibly homozygous51622650
101403733314037334GC10GENIChomozygous51622651
101403920514039206TC18GENIChomozygous51622652
101404111414041115AATGTGTGTGTAGTATGTGG20GENIChomozygous52313039
101404375314043754AG11GENIChomozygous51622655
101404423614044237TC29GENIChomozygous51622656
101404493714044941TTTG----22GENIChomozygous51622657
101404532914045330GA17GENIChomozygous51622658
101404540014045401TTTCCTGGGAGC20GENIChomozygous51622659
101404104614041054GTGTGTGT--------10GENICheterozygous52481274
101404104814041054GTGTGT------10GENICheterozygous52481276