chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------13GENIChomozygous695886694
85378107053781071CT30GENIChomozygous534703488
85378121053781211AG43GENIChomozygous534703489
85378128753781288GGAA18GENICheterozygous695886695
85378128753781288GGAAA18GENICheterozygous695886696
85378128753781288GGA18GENICheterozygous695886697
85378133353781334AG50GENIChomozygous534703490
85378146653781467AG54GENIChomozygous534703491
85378180553781806AG44GENIChomozygous534703492
85378193153781932TTTTA16GENICheterozygous695886698
85378193153781932TTTA16GENICheterozygous695886699
85378200853782013GTTTG-----25GENIChomozygous695886700
85378201253782013G-29GENICheterozygous695886701
85378241353782414CT50GENIChomozygous534703493
85378260753782608TC36GENIChomozygous534703494
85378277053782771GA43GENICpossibly homozygous534703495
85378331953783320AG56GENIChomozygous534703496
85378340253783403T-28GENIChomozygous695886702
85378373853783739GT52GENIChomozygous534703497
85378379353783794TC39GENICpossibly homozygous534703498
85378391753783918T-19GENICheterozygous695886703
85378391953783926TGCGTGT-------22GENICheterozygous695886704
85378393753783938TC33GENICheterozygous534703499
85378404853784049TC51GENIChomozygous534703500
85378550553785506T-13GENIChomozygous695886705
85378550753785508TTTTTTTC13GENICheterozygous695886706
85378552153785522CCTTTT10GENIChomozygous695886708