chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38052996780529968TC72GENICpossibly homozygous111635507
38053048180530482GA83GENICpossibly homozygous111635508
38053121380531214CT54GENIChomozygous111950441
38053123880531239AG47GENIChomozygous111635510
38053330980533310TC37GENICheterozygous111950443
38053331080533311GA36GENICheterozygous111950445
38053331480533315TC36GENICheterozygous111950447
38053332180533322CT37GENICheterozygous111950449
38053432680534327AG43GENIChomozygous111635516
38053499980535000TC67GENIChomozygous111635517
38053696680536967CT55GENIChomozygous111635518
38053782880537829TC45GENIChomozygous111635519
38053875080538751CT48GENIChomozygous111635520
38053931980539320GA57GENIChomozygous111635521
38054002380540024GA63GENIChomozygous111635522
38054011580540116TA50GENIChomozygous111635523
38054019580540196CT49GENIChomozygous111635524
38054023580540236CT57GENIChomozygous111635525
38054026280540263CA56GENIChomozygous111635526
38054033580540336CA52GENIChomozygous111635527
38054098980540990TC52GENIChomozygous111635528
38054103980541040CT62GENIChomozygous111635529
38054163780541638CT40GENIChomozygous111635530
38054297480542975GA51GENIChomozygous111635531