chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104657129946571300GA56GENIChomozygous116877803
104657144346571443AG58GENIChomozygous128814348
104657477246574772GGTGGCTCAGC43GENIChomozygous128814349
104657223346572234TC74GENIChomozygous116586256
104657432146574322CT43GENIChomozygous116931444
104657492846574929A33GENICheterozygous131092565
104657795446577955TG59GENIChomozygous116586274
104657876646578767AG67GENICpossibly homozygous116586276
104658005446580055GA53GENIChomozygous116931446
104658075046580751TC62GENIChomozygous116586278
104658125346581254CT49GENIChomozygous116931448
104658234646582347CT52GENICpossibly homozygous116931450
104658447046584471AG43GENIChomozygous116586292
104658478646584787AT38GENIChomozygous116586294
104658641646586417TC53GENIChomozygous116586300
104658749846587499AG34GENICpossibly homozygous116931452
104658803746588044CCCCCTA11GENIChomozygous128814356
104658805146588061TCCCCCCCAC12GENIChomozygous128814357
104658872946588730GA56GENIChomozygous116931454
104658928746589288TC49GENIChomozygous116931456
104658963346589634TG36GENIChomozygous116586310
104658117946581179ATATCC39GENIChomozygous132691597