chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72631024926310250CT47GENIChomozygous115623894
72631175626311757AC49GENIChomozygous115623899
72631841926318420CT22GENIChomozygous115623929
72631956426319564AAGATA35GENIChomozygous128444624
72632105226321052AC32GENIChomozygous134213363
72631551726315518TC43GENIChomozygous116363405
72632284326322844GA52GENIChomozygous116363407
72632714326327144AT63GENIChomozygous116363408
72633465326334654TA50GENIChomozygous115623995
72633484126334841TTAAAGTCAGTTCTTATATTTTTGGTTGTGAGCCTAGCCTTTAACGGCTGAGCCATCTCTCCAGCCC30GENIChomozygous128444635
72633572426335725GA55GENIChomozygous116324809
72633595626335957AG43GENIChomozygous115624003
72633732726337328GA37GENIChomozygous116363409
72634110726341108A37GENIChomozygous128444640
72634112726341128AG45GENIChomozygous115624025
72634177826341779CT34GENIChomozygous115624032
72634313426343138AAAC27GENICheterozygous133626562
72634616026346161AG50GENIChomozygous115624048
72634657826346578T55GENICpossibly homozygous134213364
72635060326350604CT47GENIChomozygous116363410
72635176026351761CT20GENIChomozygous116363411
72635223026352230AGAG41GENIChomozygous132982283
72635244026352441TC49GENIChomozygous115624065
72635259926352600AC40GENIChomozygous115624066
72635281326352814GT30GENIChomozygous115624068
72635303926353040GA57GENIChomozygous116324823
72635328726353288GA41GENIChomozygous116363412
72635373126353732CT47GENIChomozygous116363413
72635432826354329AG35GENIChomozygous115624082
72635467126354672CG26GENICheterozygous133558069
72635468126354682CT26GENICheterozygous134291616
72635488426354885TC42GENIChomozygous115624085
72635697426356975AG37GENIChomozygous115624089
72635717226357173GA48GENICpossibly homozygous116363414
72635923526359236CT51GENIChomozygous116363415
72636008926360089G39GENICpossibly homozygous131675523
72636080926360810GC47GENIChomozygous115624100