chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403357914033583TTTT----22GENICpossibly homozygous51622641
101403406114034062TC13GENIChomozygous51622644
101403420714034208AAAT7GENIChomozygous51622645
101403433814034339A-12GENIChomozygous51622646
101403462714034628GA22GENIChomozygous51622647
101403486914034870CA26GENIChomozygous51622648
101403531514035316CCAAAA4GENICheterozygous52356527
101403675914036760A-20GENIChomozygous51622650
101403733314037334GC15GENIChomozygous51622651
101403920514039206TC30GENIChomozygous51622652
101404375314043754AG33GENIChomozygous51622655
101404423614044237TC39GENIChomozygous51622656
101404493714044941TTTG----16GENIChomozygous51622657
101404532914045330GA28GENIChomozygous51622658
101404540014045401TTTCCTGGGAGC20GENIChomozygous51622659
101403531614035319AAA---4GENICheterozygous52431569
101403531714035319AA--4GENICheterozygous52431571
101404104614041054GTGTGTGT--------16GENICheterozygous52481274
101404104814041054GTGTGT------16GENICpossibly homozygous52481276
101404111414041115AATGTGTGTGTAGTATGTGG9GENIChomozygous52313039