chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------23GENIChomozygous735704834
85378107053781071CT18GENIChomozygous610776441
85378121053781211AG24GENIChomozygous610776442
85378128753781288GGA14GENICheterozygous735704836
85378128753781288GGAA14GENICheterozygous735704837
85378128753781288GGAAA14GENICheterozygous735704838
85378133353781334AG18GENIChomozygous610776443
85378146653781467AG23GENIChomozygous610776444
85378180553781806AG21GENIChomozygous610776445
85378193153781932TTTA7GENIChomozygous735704839
85378200853782013GTTTG-----14GENIChomozygous735704842
85378241353782414CT23GENIChomozygous610776446
85378260753782608TC19GENIChomozygous610776447
85378277053782771GA19GENICpossibly homozygous610776448
85378331953783320AG30GENIChomozygous610776449
85378340253783403T-8GENIChomozygous735704843
85378373853783739GT17GENIChomozygous610776450
85378379353783794TC16GENIChomozygous610776451
85378391753783918T-14GENICpossibly homozygous735704844
85378391953783926TGCGTGT-------16GENICpossibly homozygous735704845
85378404853784049TC31GENIChomozygous610776452
85378438353784384A-20GENICpossibly homozygous735704846
85378550753785508TTTTTTTC6GENIChomozygous735704847