chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141894409141894430TTTTTTTTTTTTTTTTTTTTT---------------------17GENICheterozygous55017337
7141894426141894430TTTT----17GENICheterozygous55017339
7141894429141894430TTAA26GENICheterozygous55017341
7141894455141894456T-31GENICheterozygous54159988
7141894589141894590CCA16GENICheterozygous54159995
7141894592141894593C-16GENICheterozygous54159996
7141894621141894622AATTGT17GENICheterozygous54160000
7141894762141894763T-29GENICheterozygous54160006
7141896965141896966GA11GENIChomozygous54839177
7141897263141897264TTA21GENIChomozygous54160021
7141897299141897300TG25GENIChomozygous54160022
7141898147141898148TA12GENIChomozygous54839180
7141898357141898358AC21GENIChomozygous54839182
7141899795141899796AG19GENIChomozygous54160024
7141900086141900087CT21GENIChomozygous54160025
7141901732141901733CG21GENIChomozygous54160027
7141901745141901746CT19GENIChomozygous54839184
7141902234141902235TTACATACATACATACATAC19GENIChomozygous55017343
7141902956141902957CT18GENIChomozygous54839192
7141903441141903442GGA14GENICpossibly homozygous54160035
7141904704141904705TC14GENIChomozygous54160040
7141907488141907489GGTTT12GENICheterozygous55017345
7141907854141907855GA21GENIChomozygous54160046
7141909490141909491CT11GENIChomozygous54839194
7141911360141911361CT21GENIChomozygous54839196
7141911569141911572AGA---12GENIChomozygous54160052
7141911644141911645G-13GENIChomozygous54160054
7141911651141911652G-16GENIChomozygous54160055
7141903441141903442GGAAAAA14GENICheterozygous55180731