chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38052996780529968TC5GENIChomozygous111635507
38053048180530482GA20GENIChomozygous111635508
38053123880531239AG10GENIChomozygous111635510
38053193180531932TC29GENIChomozygous111635513
38053432680534327AG14GENIChomozygous111635516
38053499980535000TC23GENIChomozygous111635517
38053696680536967CT16GENIChomozygous111635518
38053782880537829TC22GENIChomozygous111635519
38053875080538751CT20GENIChomozygous111635520
38053931980539320GA25GENIChomozygous111635521
38054002380540024GA15GENIChomozygous111635522
38054011580540116TA14GENIChomozygous111635523
38054019580540196CT21GENIChomozygous111635524
38054023580540236CT23GENIChomozygous111635525
38054026280540263CA20GENIChomozygous111635526
38054033580540336CA15GENIChomozygous111635527
38054098980540990TC25GENIChomozygous111635528
38054103980541040CT32GENIChomozygous111635529
38054163780541638CT24GENIChomozygous111635530
38054297480542975GA25GENIChomozygous111635531
38053044680530447A14GENICheterozygous129890177
38054038280540394GAGGCAGAGGCA15GENIChomozygous127900684
38054050380540504A16GENIChomozygous127900685
38053196180531962GC25GENIChomozygous112242014
38053397280533973GC3GENIChomozygous112242016
38053409680534097AC14GENIChomozygous112242017
38053376880533768CGGGCTG2GENIChomozygous132955305
38053377180533771AGATGGCTCAGCAGTTAAGAGCACCCGAC2GENIChomozygous132955306