chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1143128047143128048GGGCCCA29GENIChomozygous60877373
1143129483143129484GGA14GENICpossibly homozygous61531627
1143131057143131058AG39GENIChomozygous61902650
1143131279143131280GC21GENIChomozygous61902651
1143132154143132155CT36GENIChomozygous61531629
1143133479143133480GA37GENIChomozygous61902652
1143134196143134197AG34GENIChomozygous60877381
1143134637143134638CG38GENIChomozygous60877382
1143135178143135179AG30GENIChomozygous60877383