chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101403357914033583TTTT----10GENICheterozygous51622641
101403406114034062TC35GENIChomozygous51622644
101403433814034339A-8GENIChomozygous51622646
101403462714034628GA13GENIChomozygous51622647
101403486914034870CA50GENIChomozygous51622648
101403531614035319AAA---6GENICheterozygous52431569
101403531714035319AA--6GENICheterozygous52431571
101403675914036760A-12GENICpossibly homozygous51622650
101403733314037334GC32GENIChomozygous51622651
101403920514039206TC49GENIChomozygous51622652
101404375314043754AG61GENIChomozygous51622655
101404423614044237TC39GENIChomozygous51622656
101404493714044941TTTG----29GENIChomozygous51622657
101404532914045330GA65GENIChomozygous51622658
101404540014045401TTTCCTGGGAGC66GENIChomozygous51622659
101404104614041054GTGTGTGT--------51GENICheterozygous52481274
101404104814041054GTGTGT------51GENICheterozygous52481276
101404105214041054GT--51GENICheterozygous52481278
101404111414041115AATGTGTGTGTAGTATGTGG45GENIChomozygous52313039