chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141894409141894430TTTTTTTTTTTTTTTTTTTTT---------------------25GENICheterozygous55017337
7141894426141894430TTTT----25GENICheterozygous55017339
7141894429141894430TTAA24GENICheterozygous55017341
7141894455141894456T-25GENICheterozygous54159988
7141894589141894590CCA35GENICheterozygous54159995
7141894592141894593C-38GENICheterozygous54159996
7141894621141894622AATTGT32GENICheterozygous54160000
7141897263141897264TTA28GENIChomozygous54160021
7141897299141897300TG30GENIChomozygous54160022
7141899795141899796AG46GENIChomozygous54160024
7141900086141900087CT24GENIChomozygous54160025
7141901732141901733CG38GENIChomozygous54160027
7141901745141901746CT39GENIChomozygous54839184
7141896965141896966GA29GENIChomozygous54839177
7141898147141898148TA43GENIChomozygous54839180
7141898357141898358AC27GENIChomozygous54839182
7141902234141902235TTACATACATACATACATAC31GENICpossibly homozygous55017343
7141902956141902957CT41GENIChomozygous54839192
7141903441141903442GGA19GENICpossibly homozygous54160035
7141904704141904705TC37GENIChomozygous54160040
7141907854141907855GA30GENIChomozygous54160046
7141909490141909491CT32GENIChomozygous54839194
7141911360141911361CT40GENIChomozygous54839196
7141911569141911572AGA---36GENIChomozygous54160052
7141911644141911645G-42GENIChomozygous54160054
7141911651141911652G-45GENIChomozygous54160055
7141907488141907489GGTTT24GENICheterozygous55017345