chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5146475599146475600CA5GENIChomozygous55773045
5146477242146477243GA15GENIChomozygous55773046
5146477618146477619TC30GENIChomozygous55773048
5146479417146479418TC40GENIChomozygous55773050
5146480090146480091GA14GENICheterozygous56126268
5146481148146481149CCAAA8GENIChomozygous55773052
5146481160146481161CA10GENICpossibly homozygous55773054
5146481621146481622GC15GENIChomozygous55773056
5146481786146481787GA26GENIChomozygous55773058
5146482146146482147AAAC12GENICheterozygous55773060
5146482146146482147AAACAC12GENICheterozygous56069654
5146482634146482635T-2GENIChomozygous55773064
5146482845146482847TT--4GENIChomozygous55773066
5146482875146482877TT--3GENICheterozygous55773068
5146483650146483651AAT22GENIChomozygous55773070
5146485001146485002TC21GENIChomozygous55773072
5146485107146485108TTTTTCTTTC4GENIChomozygous55773074
5146486575146486576T-1GENIChomozygous55773076
5146486599146486600AG16GENIChomozygous55773078
5146487526146487527CT19GENIChomozygous55773079
5146487784146487785AG24GENIChomozygous55773081
5146488580146488581AG38GENIChomozygous55773083
5146488893146488894A-6GENICheterozygous55773085
5146489420146489427AAAAAAA-------6GENICheterozygous55773087
5146490123146490124GA20GENICheterozygous55773091
5146490128146490129CT20GENICheterozygous55773093
5146490139146490140TTTA20GENICheterozygous55773095
5146490162146490163CT15GENICheterozygous55773097
5146490325146490326G-16GENIChomozygous55773099
5146490777146490778AATTTCTTTTT2GENIChomozygous55773103
5146490859146490860CT28GENICpossibly homozygous55773105
5146491339146491340TC39GENICheterozygous55773107
5146491339146491340TTGCAC28GENIChomozygous55773109
5146492641146492642AG29GENIChomozygous55773111