chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104497795544977956GT35GENIChomozygous51441478
104497881644978818CT--25GENIChomozygous51635809
104497919444979196AA--21GENIChomozygous51635810
104497942444979438GTGTGTGTGTGTGT--------------3GENIChomozygous53026127
104498221744982218TG27GENIChomozygous51635812
104498382944983830CA20GENIChomozygous51635815
104498708044987081CT27GENIChomozygous51635822
104498788144987884CCC---11GENICheterozygous52600370
104498190144981902TC28GENIChomozygous52317893
104498636744986368GGA8GENICheterozygous52799871
104498788244987884CC--11GENICheterozygous52799873
104498399644984006ACACACACAC----------8GENICheterozygous52372805
104498399844984006ACACACAC--------8GENICheterozygous52372807
104499051744990518A-29GENIChomozygous51635823
104499192844991930CC--15GENIChomozygous51635824
104499201544992016G-23GENIChomozygous51635825
104499233544992336TC25GENIChomozygous51441536
104499233944992340CT23GENIChomozygous51635826
104499237344992374AG19GENIChomozygous51635827
104499289144992892CCAAA6GENICheterozygous51441537
104499337144993372AAGAG23GENIChomozygous51441539
104499438144994382CCAAGAAGTACAGAACCTTAGAGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAGAACCA21GENIChomozygous53026130
104499650844996509CCCTGT22GENIChomozygous51441548
104499654144996542AG31GENIChomozygous51635829
104499686444996865TG29GENIChomozygous51635830
104499762244997623AG33GENIChomozygous51441550
104499776544997766TC11GENIChomozygous51441551
104499777244997773GGA6GENIChomozygous51635831
104499818744998188TTAA19GENICpossibly homozygous51635832
104499837944998380GA26GENIChomozygous51635833
104499918144999182TC19GENIChomozygous51441553
104499986144999862TC32GENIChomozygous51441554
104499565844995664ATAAAT------3GENIChomozygous52722756
104499193444991935CT14GENIChomozygous52934413