chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84769553947695543GATA----10GENICpossibly homozygous53270579
84769564247695643TTA11GENICpossibly homozygous52620706
84769588647695894GTGTGTGT--------6GENICheterozygous53429499
84769588847695894GTGTGT------6GENICheterozygous53429501
84769750647697507GGA7GENICheterozygous52620708
84769750647697507GGAA7GENICheterozygous53429505
84769753347697534GA10GENIChomozygous52620710
84769754847697549AAGT12GENICpossibly homozygous52620712
84769833047698331GGTTC2GENICheterozygous53429508
84769863647698637AG16GENIChomozygous52620714
84770026647700267GC30GENICpossibly homozygous52620716
84770097947700980CT24GENIChomozygous52620718
84770135147701352TTA14GENIChomozygous52620720
84770188947701890AG15GENIChomozygous52620722
84770356647703567AG20GENIChomozygous52620726
84770452847704529TTG19GENIChomozygous52620728
84770802847708029CG20GENIChomozygous52620730
84770839447708395CT21GENIChomozygous52620732
84770907947709080TA20GENIChomozygous52620734
84770919447709195CG24GENIChomozygous52620736
84771004647710047GA29GENIChomozygous52620738
84771069747710698AT18GENIChomozygous52620740
84771154847711549AG18GENIChomozygous52620742
84771598447715985GA20GENIChomozygous52620744
84771616547716166TC24GENIChomozygous52620746