chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------8GENIChomozygous690944849
85378107053781071CT34GENIChomozygous521521571
85378121053781211AG38GENIChomozygous521521572
85378128753781288GGAA19GENICheterozygous690944850
85378128753781288GGAAA19GENICheterozygous690944851
85378133353781334AG37GENIChomozygous521521573
85378146653781467AG36GENIChomozygous521521574
85378180553781806AG41GENIChomozygous521521575
85378193153781932TTTTA20GENICheterozygous690944853
85378193153781932TTTA20GENICheterozygous690944854
85378200853782013GTTTG-----39GENIChomozygous690944855
85378201253782013G-40GENICpossibly homozygous690944856
85378241353782414CT29GENIChomozygous521521576
85378260753782608TC40GENIChomozygous521521577
85378277053782771GA15GENIChomozygous521521578
85378331953783320AG48GENIChomozygous521521579
85378340253783403T-28GENIChomozygous690944857
85378373853783739GT56GENIChomozygous521521580
85378379353783794TC48GENIChomozygous521521581
85378391753783918T-17GENICheterozygous690944858
85378391953783926TGCGTGT-------16GENICheterozygous690944859
85378393753783938TC18GENICheterozygous521521582
85378404853784049TC36GENIChomozygous521521583
85378550553785506T-23GENIChomozygous690944860
85378550753785508TTTTTTTC26GENICpossibly homozygous690944861
85378552153785522CCTTTT17GENIChomozygous690944863