chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403357914033583TTTT----13GENICpossibly homozygous51622641
101403406114034062TC8GENIChomozygous51622644
101403420714034208AAAT9GENIChomozygous51622645
101403433814034339A-7GENIChomozygous51622646
101403462714034628GA12GENIChomozygous51622647
101403486914034870CA25GENIChomozygous51622648
101403531614035319AAA---6GENICheterozygous52431569
101403531714035319AA--6GENICheterozygous52431571
101403675914036760A-23GENIChomozygous51622650
101403733314037334GC27GENIChomozygous51622651
101403920514039206TC24GENIChomozygous51622652
101404104614041054GTGTGTGT--------10GENICheterozygous52481274
101404104814041054GTGTGT------10GENICpossibly homozygous52481276
101404111414041115AATGTGTGTGTAGTATGTGG7GENIChomozygous52313039
101404375314043754AG34GENIChomozygous51622655
101404423614044237TC30GENIChomozygous51622656
101404493714044941TTTG----22GENIChomozygous51622657
101404532914045330GA35GENIChomozygous51622658
101404540014045401TTTCCTGGGAGC30GENIChomozygous51622659