chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
178995675089956751TC15GENIChomozygous111141442
178995891589958916TC20GENICheterozygous119419633
178996025889960259CT28GENICpossibly homozygous111141444
178996377289963773CA14GENIChomozygous111141446
178996833389968334CG8GENIChomozygous111141450
178997204389972044GA28GENIChomozygous111141452
178997291589972916CT16GENIChomozygous111141454
178997590489975905TG13GENIChomozygous111141456
178997670689976707AC14GENIChomozygous111141458
178997865289978653AG22GENIChomozygous111141462
178998073489980735TC11GENIChomozygous111141464
178998098189980982CG20GENIChomozygous111141466
178998839389988394CT18GENIChomozygous111141468
178999129989991300GT9GENIChomozygous111141470
178999175889991759AG7GENIChomozygous111141471
178999506189995062TC9GENIChomozygous111141473
178999644789996448GA21GENIChomozygous111141475
179001129790011298AC14GENIChomozygous111141477
179001392990013930TC16GENIChomozygous111141479
179001583690015837AG18GENIChomozygous111141481
179001594590015946CT21GENIChomozygous111141482
179001629290016293GC15GENIChomozygous111141484
179001663890016639CT29GENICpossibly homozygous111141486
179002142590021426CT13GENIChomozygous111141488
179002313190023132CT15GENIChomozygous111141490
179002359290023593TA39GENIChomozygous111141492
179003159290031593AC19GENICheterozygous119314625
178997769889977699AG36GENICpossibly homozygous111225342
179000064390000644AG11GENIChomozygous111225343
179003149490031495AT11GENIChomozygous111225344
179002614290026143CT16GENIChomozygous111504674