chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------28GENIChomozygous705329895
85378107053781071CT21GENIChomozygous557460577
85378121053781211AG17GENIChomozygous557460578
85378128753781288GGAA8GENICheterozygous705329898
85378128753781288GGAAA8GENICpossibly homozygous705329899
85378133353781334AG8GENIChomozygous557460579
85378146653781467AG20GENIChomozygous557460580
85378180553781806AG19GENIChomozygous557460581
85378193153781932TTTA11GENICheterozygous705329900
85378193153781932TTTTA11GENICheterozygous705329901
85378200853782013GTTTG-----11GENIChomozygous705329903
85378241353782414CT23GENIChomozygous557460582
85378260753782608TC21GENIChomozygous557460583
85378268153782682GGGTGT1GENIChomozygous705329904
85378277053782771GA9GENIChomozygous557460584
85378331953783320AG24GENIChomozygous557460585
85378340253783403T-13GENIChomozygous705329905
85378373853783739GT28GENIChomozygous557460586
85378379353783794TC19GENIChomozygous557460587
85378391753783918T-12GENIChomozygous705329906
85378391953783926TGCGTGT-------13GENIChomozygous705329907
85378404853784049TC33GENIChomozygous557460588
85378552153785522CCTTTT5GENIChomozygous705329909