chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9105690736105690737AT54GENIChomozygous138648368
9105691229105691229A58GENIChomozygous138478346
9105691908105691909C48GENIChomozygous138478347
9105692395105692396GA49GENIChomozygous138648369
9105695751105695752GC60GENIChomozygous138648370
9105696481105696482GA66GENIChomozygous138648371
9105699144105699144A43GENICpossibly homozygous138478348
9105701266105701268AA59GENIChomozygous138478349
9105701435105701436TC44GENIChomozygous138648372
9105702408105702409AC52GENIChomozygous138648373
9105703128105703129GA63GENIChomozygous138648374
9105706561105706561AT36GENIChomozygous138478351
9105707204105707204CC51GENIChomozygous138478352
9105708540105708541TC61GENIChomozygous138648375
9105709182105709183TC55GENIChomozygous138648376
9105710294105710295TC49GENIChomozygous138648377