chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------27GENIChomozygous752021042
85378107053781071CT15GENIChomozygous641626332
85378121053781211AG17GENIChomozygous641626333
85378128753781288GGAA23GENICheterozygous752021045
85378128753781288GGAAA23GENICheterozygous752021046
85378133353781334AG31GENIChomozygous641626334
85378146653781467AG23GENIChomozygous641626335
85378180553781806AG21GENIChomozygous641626336
85378193153781932TTTA7GENICheterozygous752021047
85378193153781932TTTTA7GENICpossibly homozygous752021048
85378200853782013GTTTG-----13GENIChomozygous752021050
85378241353782414CT15GENIChomozygous641626337
85378260753782608TC12GENIChomozygous641626338
85378268153782682GGGTGT2GENIChomozygous752021051
85378277053782771GA6GENIChomozygous641626339
85378331953783320AG15GENIChomozygous641626340
85378340253783403T-12GENIChomozygous752021052
85378373853783739GT20GENIChomozygous641626341
85378379353783794TC22GENICpossibly homozygous641626342
85378391753783918T-11GENIChomozygous752021053
85378391953783926TGCGTGT-------11GENIChomozygous752021054
85378404853784049TC16GENIChomozygous641626343
85378550553785506T-5GENIChomozygous752021055
85378552153785522CCTTTT6GENIChomozygous752021057