chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104657129946571300GA54GENIChomozygous116877803
104657144346571443AG70GENIChomozygous128814348
104657469846574699GA57GENIChomozygous116877805
104657477246574772GGTGGCTCAGC59GENIChomozygous128814349
104657527846575279GT79GENIChomozygous116877807
104657783646577837GA65GENIChomozygous116877809
104657795446577955TG76GENIChomozygous116586274
104657876646578767AG78GENIChomozygous116586276
104658075046580751TC55GENIChomozygous116586278
104658388446583885CT64GENIChomozygous116877813
104658447046584471AG64GENIChomozygous116586292
104658478646584787AT55GENIChomozygous116586294
104658580646585807CT81GENIChomozygous116877815
104658641646586417TC61GENIChomozygous116586300
104657492846574929A54GENICpossibly homozygous131092565
104657971546579738AGGATAGCCCACAGCAGGGCCAT48GENICpossibly homozygous131092566
104658803746588044CCCCCTA22GENIChomozygous128814356
104658805146588061TCCCCCCCAC22GENIChomozygous128814357
104659139046591391TC60GENIChomozygous116877819
104658825346588254GA63GENIChomozygous117008775