chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
678975777897578CT36GENIChomozygous54290107
678983467898347CT32GENIChomozygous54290108
678993677899368CT48GENICpossibly homozygous54290109
678994027899403AG57GENICpossibly homozygous54290110
678994037899404CCGT52GENICpossibly homozygous54290111
679000037900004TC23GENIChomozygous54290112
679004717900472GA39GENIChomozygous54290113
679007547900755TC4GENIChomozygous54290114
679009707900971CCAT2GENIChomozygous54290115
679013117901312AG26GENIChomozygous54290116
679022137902214AACC6GENIChomozygous54290117
679032147903215AG19GENICpossibly homozygous54290118
679032167903217GA18GENICpossibly homozygous54290119
679032347903236GT--14GENIChomozygous54290120
679032917903292CT16GENIChomozygous54290122
679035577903558AG41GENIChomozygous54290123
679036957903696CT24GENIChomozygous54290124
679037727903773AG32GENICpossibly homozygous54290125
679039257903926AT15GENIChomozygous54290126
679043027904303CT45GENICheterozygous54290127
679046287904629AC50GENIChomozygous54290128
679049187904919GA22GENIChomozygous54290129
679050567905058TA--6GENICheterozygous54290130
679056387905639GA28GENICpossibly homozygous54290131
679061567906157TC34GENIChomozygous54290132
679065467906547CA42GENIChomozygous54290133
679073937907394AAAC22GENIChomozygous54290136
679074677907471CACT----55GENIChomozygous54290137
679078637907871CTCTGTGT--------9GENICpossibly homozygous54290138
679078637907875CTCTGTGTGTGT------------9GENICheterozygous54814218
679088557908856AAC26GENICpossibly homozygous54290139
679099127909918TCTCTA------14GENIChomozygous54290140
679100567910057GGTC28GENICpossibly homozygous54290141
679101437910144GGTCTGTC10GENIChomozygous54290142
679101437910144GC26GENICheterozygous54814224
679101777910178AG20GENICheterozygous54814226
679102117910215TCTC----6GENICheterozygous54290143
679109427910943GA35GENIChomozygous54290144
679113507911351TC44GENIChomozygous54290145