chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104497795544977956GT8GENIChomozygous51441478
104498190144981902TC5GENIChomozygous52317893
104498221744982218TG6GENIChomozygous51635812
104497881644978818CT--6GENIChomozygous51635809
104497919444979196AA--6GENIChomozygous51635810
104498382944983830CA14GENIChomozygous51635815
104498399844984006ACACACAC--------5GENIChomozygous52372807
104498523744985319CACTCGAGTGGATGGGATTCCCACTCCGTTGTTTTTGAGTGCACTCGGGTGGATGGGCTTCCCACCCCGTTGTTTTTGAGTA----------------------------------------------------------------------------------6GENICheterozygous53309313
104498708044987081CT8GENIChomozygous51635822
104498788244987884CC--6GENICheterozygous52799873
104498636744986368GGA2GENIChomozygous52799871
104498788344987884C-6GENICheterozygous52799875
104499051744990518A-4GENIChomozygous51635823
104499192844991930CC--10GENIChomozygous51635824
104499193444991935CT10GENIChomozygous52934413
104499201544992016G-11GENIChomozygous51635825
104499233544992336TC13GENIChomozygous51441536
104499233944992340CT13GENIChomozygous51635826
104499237344992374AG7GENIChomozygous51635827
104499337144993372AAGAG5GENIChomozygous51441539
104499438144994382CCAAGAAGTACAGAACCTTAGAGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAGAACCA8GENIChomozygous53026130
104499565844995664ATAAAT------3GENIChomozygous52722756
104499650844996509CCCTGT5GENIChomozygous51441548
104499654144996542AG7GENIChomozygous51635829
104499686444996865TG9GENIChomozygous51635830
104499717444997176CA--4GENICheterozygous53026133
104499762244997623AG7GENIChomozygous51441550
104499776544997766TC4GENIChomozygous51441551
104499777244997773GGA4GENIChomozygous51635831
104499818744998188TTAA7GENIChomozygous51635832
104499837944998380GA10GENIChomozygous51635833
104499918144999182TC4GENIChomozygous51441553
104499986144999862TC4GENIChomozygous51441554