chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104657129946571300GA10GENIChomozygous116877803
104657144346571443AG12GENIChomozygous128814348
104657469846574699GA18GENIChomozygous116877805
104657477246574772GGTGGCTCAGC17GENIChomozygous128814349
104657527846575279GT13GENIChomozygous116877807
104657783646577837GA16GENIChomozygous116877809
104657795446577955TG17GENIChomozygous116586274
104657876646578767AG10GENIChomozygous116586276
104658075046580751TC6GENIChomozygous116586278
104658388446583885CT8GENIChomozygous116877813
104658447046584471AG9GENIChomozygous116586292
104658478646584787AT9GENIChomozygous116586294
104658580646585807CT14GENIChomozygous116877815
104658641646586417TC10GENIChomozygous116586300
104657492846574929A15GENICpossibly homozygous131092565
104657971546579738AGGATAGCCCACAGCAGGGCCAT12GENIChomozygous131092566
104658803746588044CCCCCTA1GENIChomozygous128814356
104658805146588061TCCCCCCCAC1GENIChomozygous128814357
104659139046591391TC14GENIChomozygous116877819
104658825346588254GA13GENIChomozygous117008775