chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104657129946571300GA62GENIChomozygous116877803
104657144346571443AG66GENIChomozygous128814348
104657469846574699GA64GENICpossibly homozygous116877805
104657477246574772GGTGGCTCAGC59GENIChomozygous128814349
104657527846575279GT77GENICpossibly homozygous116877807
104657492846574929A42GENICpossibly homozygous131092565
104657783646577837GA78GENIChomozygous116877809
104657795446577955TG59GENIChomozygous116586274
104657876646578767AG81GENIChomozygous116586276
104657971546579738AGGATAGCCCACAGCAGGGCCAT61GENIChomozygous131092566
104658075046580751TC39GENIChomozygous116586278
104658388446583885CT68GENIChomozygous116877813
104658447046584471AG71GENIChomozygous116586292
104658478646584787AT69GENIChomozygous116586294
104658580646585807CT69GENIChomozygous116877815
104658641646586417TC78GENIChomozygous116586300
104658803746588044CCCCCTA25GENIChomozygous128814356
104658805146588061TCCCCCCCAC25GENIChomozygous128814357
104659139046591391TC74GENIChomozygous116877819
104658825346588254GA80GENIChomozygous117008775