chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131841339131841340AG53GENIChomozygous929152118
5131842186131842187AC39GENIChomozygous929152119
5131842813131842814GA20GENIChomozygous929152120
5131844777131844778GA53GENIChomozygous929152121
5131845402131845403CT45GENIChomozygous929152122
5131845727131845728CA39GENIChomozygous929152123
5131846180131846181TG31GENIChomozygous929152124
5131852932131852933CA30GENIChomozygous929152125
5131853410131853411AG46GENIChomozygous929152126
5131853511131853512TG57GENIChomozygous929152127
5131853678131853679TC39GENIChomozygous929152128
5131854297131854298CA44GENIChomozygous929152129
5131855380131855381CG54GENIChomozygous929152130
5131859483131859484TC44GENIChomozygous929152131
5131859936131859937GA50GENIChomozygous929152132
5131861443131861444GT35GENIChomozygous929152133
5131862290131862291CG46GENIChomozygous929152134
5131864052131864053CT23GENIChomozygous929152135